SUN PHARMACEUTICAL INDUSTRIES INC recalls
Every recall we track for SUN PHARMACEUTICAL INDUSTRIES INC — 140 in all, from 2013–2026 — plus the complaints and injury reports the public filed about them. 4 are rated “stop using now”.
Recalls per year, by danger level
Recalls from SUN PHARMACEUTICAL INDUSTRIES INC peaked in 2022 (20); 130 since 2017. 3% rated “stop using now”.
All FDA recall records for SUN PHARMACEUTICAL INDUSTRIES INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 1 | 0 | 4 | 4 | 9 |
| 2018 | 0 | 1 | 6 | 1 | 8 |
| 2019 | 1 | 1 | 5 | 2 | 9 |
| 2020 | 0 | 1 | 6 | 0 | 7 |
| 2021 | 1 | 1 | 10 | 2 | 14 |
| 2022 | 0 | 3 | 12 | 5 | 20 |
| 2023 | 0 | 3 | 10 | 3 | 16 |
| 2024 | 0 | 0 | 6 | 12 | 18 |
| 2025 | 0 | 0 | 12 | 3 | 15 |
| 2026 (to date) | 1 | 2 | 4 | 7 | 14 |
SUN PHARMACEUTICAL INDUSTRIES INC recalls before 2017
Recalls on record by year.
Most common reasons for SUN PHARMACEUTICAL INDUSTRIES INC recalls
What to do if you have a recalled SUN PHARMACEUTICAL INDUSTRIES INC product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All SUN PHARMACEUTICAL INDUSTRIES INC recalls
60 shown- Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro
Northstar Rx LLC recalls specific lots of Tretinoin Cream USP 0.05% due to failed impurity specifications. Check your lot number immediately.
Northstar RxSep 25, 2026 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd.,
Sun Pharmaceutical recalls 200mg Carbamazepine tablets with black spots caused by burnt excipients during manufacturing. Rx-only medication distributed by Taro Pharmaceuticals USA. No remedy specified in official notice.
Sun Pharmaceutical IndustriesAug 3, 2026 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel
Sun Pharmaceutical recalls Perampanel CIII 6mg tablets due to label mix-up with 10mg tablets. Affected units contain incorrect labeling that may lead to incorrect dosing.
Sun PharmaceuticalJun 17, 2026 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm
Sun Pharmaceutical recalls 180mg fexofenadine tablets due to failed impurities and degradation specifications. Affected lots expire by March 2027 or October 2026. Consumers should check NDC codes and lot numbers.
Sun Pharmaceutical IndustriesJun 1, 2026 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Budesonide Inhalation Suspension, 1mg/2mL, 30 x 2 mL Sterile Single-Dose Ampules (5 Single-Dose Ampules per pouch, 6
Sun Pharmaceutical recalls specific lots of Budesonide Inhalation Suspension due to black/brown specs. Check your NDC and lot number for details.
Sun Pharmaceutical IndustriesMay 29, 2026 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories
Sun Pharmaceutical recalls Xyvona 2mg tablets due to FDA denial of marketing under the proprietary name. Check lot AD93852.
XyvonaMay 22, 2026 - Stop using nowDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-dose vials, Sterile, Rx only,
Sun Pharmaceutical recalls DOXOrubin Hydrochloride Liposome injections due to glass particles. This may cause serious injury if injected. Affected lots: HAG2581B, expires 05/31/2027.
Sun PharmaceuticalMay 12, 2026 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T
Sun Pharmaceutical Industries recalls 0.05% Fluocinonide cream due to failed viscosity tests. This may affect stability and product performance. Contact for details.
Sun Pharmaceutical IndustriesMar 25, 2026 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Diclofenac Sodium, Topical Gel, 3%, 100 g tube, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada
Sun Pharmaceutical Industries recalls Diclofenac Sodium Topical Gel 3% due to failed viscosity specifications. This may affect product stability and effectiveness.
Sun Pharmaceutical IndustriesJan 27, 2026 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinolone Acetonide Solution Topical Solution USP, 0.01%, 60-mL bottles, Rx only, Dist. by: Taro Pharmaceuticals
Sun Pharmaceutical recalls 0.01% Fluocinolone Acetonide Solution Topical Solution bottles due to impurity D. This may affect safety for patients using prescription steroid creams.
Sun Pharmaceutical IndustriesDec 30, 2025 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Clindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle, Rx only, Mfd. by: Taro
SUN PHARMACEUTICAL recalls Clindamycin Phosphate topical solution due to impurities and degradation. This medication is prescription-only and may pose risks if used improperly.
SUN PHARMACEUTICAL INDUSTRIES INCNov 26, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New
Sun Pharmaceutical recalls 60mg Lisdexamfetamine Dimesylate capsules with failed dissolution tests. This may affect medication stability. Contact for return instructions.
Sun PharmaceuticalOct 28, 2025 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Kit for the Preparation of Technetium Tc 99m Mertiatide, Rx Only, Manufactured by: Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical recalls Mertiatide kits with failed dissolution specifications due to sulfate issues in Sodium Tartrate Dihydrate. This affects specific lots and NDC numbers. Contact for details.
Sun PharmaceuticalSep 3, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida BioPharm, Inc., 1100 Orthodox St,
Sun Pharmaceutical recalls 25mg spironolactone tablets with aluminum foreign substance. This could cause harm if ingested. Contact Sun Pharmaceutical for details.
Sun PharmaceuticalAug 5, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles, Rx only, Manufactured by: OHM Laboratories, New
Sun Pharmaceuticals recalls 60mg lisdexamfetamine capsules (NDC 57664-051-88) due to failed dissolution tests at 9 months. This may affect drug stability and safety.
Sun PharmaceuticalsJun 16, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles,
Sun Pharmaceutical recalls 500-count and 1000-count Gabapentin 400mg capsules due to cross contamination risk. Affected lots expire March 2025. Consumers should check NDC codes and lot numbers.
Sun PharmaceuticalMar 4, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc.,
Sun Pharmaceutical recalls 100mg Morphine Sulfate Extended-Release Tablets (100-count) due to failed dissolution specifications. This may affect medication effectiveness. Check NDC 63304-452-01 and lot number AD16615.
Sun PharmaceuticalFeb 6, 2025 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Nitrofurantoin Capsules, USP (Macrocrystals), 100 mg, Rx Only, 100 capsules per bottle, Manufactured by: Sidmak
Sun Pharmaceutical recalls Nitrofurantoin Capsules (100mg) due to failed dissolution specifications. This may affect medication effectiveness. Check NDC 57664-233-88 and lot numbers 231067, 231069.
Sun PharmaceuticalJul 9, 2024 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Decitabine for Injection 50mg per vial, For intravenous infusion only Cytotoxic Agent, Sterile, Rx Only, Single-Dose
Sun Pharmaceutical recalls Decitabine injection vials due to potential microbial contamination. This drug is for IV use only and requires a prescription. Affected units have specific NDC and expiration dates.
Sun PharmaceuticalJul 2, 2024 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun
Sun Pharmaceutical recalls Xelpros (latanoprost) 0.005% ophthalmic emulsion due to particulate matter test failure. This may cause eye irritation or injury. Affected units have specific NDC and lot numbers.
Sun PharmaceuticalApr 22, 2024 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Amphotericin B Liposome for Injection, 50mg vials, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical recalls 50mg Amphotericin B Liposome vials (NDC 62756-233-01) due to assay out of specification. This may affect drug effectiveness. Contact the manufacturer for details.
Sun PharmaceuticalApr 19, 2024 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Febuxostat Tablets 80mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN
Sun Pharmaceutical recalls Febuxostat 80mg tablets due to microbial contamination in manufacturing equipment. This recall affects RX-only products with NDC 16714-060-01, lot DNE0894A, expiring 07/31/2025. Consumers should check their bottles for the specific lot number.
Sun PharmaceuticalMar 4, 2024 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Mesalamine Extended-Release Capsules, USP 500mg, Rx Only, 120 Capsules per bottle, Manufactured by: Sun Pharmaceutical
Sun Pharmaceutical recalls 500mg Mesalamine Extended-Release Capsules due to failed dissolution specifications. This may affect drug effectiveness. Check NDC 63304-089-13 and lot numbers for affected batches.
Sun PharmaceuticalFeb 5, 2024 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Lurasidone Hydrochloride Tablets 60mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries,
Sun Pharmaceutical recalls 60mg Lurasidone Hydrochloride tablets due to microbial contamination in manufacturing equipment. This could pose health risks if the tablets are taken. Consumers should check NDC 47335-639-83 and lot number DNE0620A.
Sun PharmaceuticalJan 18, 2024 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical recalls 100-count Liothyronine Sodium Tablets (5 mcg) due to failed impurities and degradation specifications. Rx-only medication distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ.
Sun PharmaceuticalDec 4, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg, 60 Tablets bottle, Distributed by: Sun
Sun Pharmaceutical recalls 200mg bupropion extended-release tablets due to failed dissolution specifications. This may affect product effectiveness. Consumers should contact Sun for details.
Sun PharmaceuticalNov 22, 2023 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Liothyronine Sodium Tablets, USP, 5 mcg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries,
Sun Pharmaceutical recalls 5 mcg Liothyronine Sodium Tablets due to failed impurities and degradation specifications. Rx-only product with NDC 62756-589-88, lot DND0058A, exp 12/2023. Consumers should contact pharmacy for safe handling.
Sun PharmaceuticalOct 20, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg, 60 tablets bottle, Rx Only, Distributed by: Sun
Sun Pharmaceutical recalls 150mg Bupropion Hydrochloride Extended-Release Tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact Sun for details.
Sun PharmaceuticalOct 4, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)),
Sun Pharma recalls Cequa (cyclosporine ophthalmic solution) 0.09% due to subpotent results. This may affect medication effectiveness. Check NDC 47335-506-96, lots 10026/10027, expiring 09/2023.
Sun PharmaSep 7, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited,
Sun Pharmaceutical recalls 500 mcg Dofet: 60-count bottles due to content uniformity testing failures. This may affect medication accuracy. Contact for return instructions.
Sun PharmaceuticalJul 18, 2023 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories
Sun Pharmaceutical recalls 20mg methylphenidate tablets with metal embedded in some tablets. This could cause injury if swallowed. Consumers should contact the company for details.
Sun PharmaceuticalJul 13, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Tiagabine Hydrochloride Tablets, 2 mg, 30-count bottle, Distributed by Sun Pharmaceutical Industries. Inc. Cranbury NJ
Sun Pharmaceutical recalls 2mg Tiagabine tablets due to failed impurities testing. This may affect safety but does not cause immediate harm. Check NDC 62756-2:200-83 for affected lots.
Sun PharmaceuticalJul 10, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Loteprednol Etabonate Ophthalmic Suspension, 5 mg/mL (0.5%), packaged as one bottle in a carton in a) 10 mL bottle
Sun Pharmaceutical recalls Loteprednol Etabonate Ophthalmic Suspension due to out of specification unit dose content. This may affect eye safety. Contact for details.
Sun PharmaceuticalJul 5, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury,
Sun Pharmaceutical recalls Amphotericin B Liposome injections due to subpotent drug levels. This may reduce effectiveness for serious fungal infections. Patients with prescribed treatment should contact their doctor.
Sun PharmaceuticalMay 30, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPrion Hydrochloride Extended-Release Tablets, USP (SR) 150 mg, 60 Tablets, Rx Only, Distributed by: Sun
Sun Pharmaceutical recalls 150mg buPROPrion Hydrochloride Extended-Release Tablets (NDC 47335-737-86) that failed dissolution testing during stability checks. This could affect medication effectiveness.
Sun PharmaceuticalMay 9, 2023 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Buprenorphine Sublingual Tablets, 8 mg, 30 count-bottles, Rx only, Manufactured by: Sun Pharma, NDC 62756-460-83.
Sun Pharma recalls 8mg buprenorphine sublingual tablets due to CGMP deviations. Affected lots may have quality issues affecting safety.
Sun PharmaMay 3, 2023 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Norepinephrine Bitartrate Injection, USP, 4 mg/4 mL* (1 mg/mL), 4 mL Single-dose Fliptop Vial (NDC 47335-615-40);
Sun Pharmaceutical recalls specific lots of Norepinephrine Bitartrate Injection due to failed impurity specifications. Check your lot numbers immediately.
Sun PharmaceuticalMar 29, 2023 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Dofetilide Capsules, 500 mcg (0.5 mg), 60-count bottle, Rx only, Manufactured by: Sun Pharmaceutical Industries
Sun Pharmaceutical recalls 500 mcg Dofetilide capsules due to failed content uniformity. This may affect medication accuracy. Contact for return instructions.
Sun PharmaceuticalMar 9, 2023 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Diltiazem Hydrochloride Extended-Release Capsules, USP, 360 mg; Rx only; 90-count bottles, Manufactured by: Sun
Sun Pharmaceutical recalls 360mg Diltiazem Hydrochloride Extended-Release Capsules due to failed impurity and dissolution testing. Rx-only bottles with specific lot numbers and expiration dates are affected.
Sun PharmaceuticalJan 13, 2023 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Oxcarbazepine Tablets 600mg, packaged in a) 100- count bottles (NDC 62756-185-88), b) 500-count bottles (NDC
Sun Pharmaceutical recalls 600mg Oxcarbazepine tablets with foreign substance risk. Affected lots expire 03/2023. Stop using and contact for remedy.
Sun PharmaceuticalDec 1, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles, Rx only, Distributed by: Sun Pharmaceutical
Sun Pharmaceutical recalls 8mg/2mg buprenorphine and naloxone sublingual tablets due to foreign substance presence. Rx-only 30-count bottles with specific lot numbers and expiration dates.
Sun PharmaceuticalOct 18, 2022 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Pantoprazole Sodium for Delayed-Release Oral Suspension*40 mg* suspension in apple juice or applesauce only Each packet
Sun Pharmaceutical recalls Pantoprazole Sodium 40mg packets (Lot MHC1317A) due to discoloration. Check your medication and contact the manufacturer for details.
Sun Pharmaceutical IndustriesJul 25, 2022 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets, Distributed by: Sun Pharmaceutical
Sun Pharmaceutical recalls 9,552 bottles of Divalproex Sodium Delayed-Release Tablets 500mg due to failed dissolution specifications. Check your lot number.
Sun PharmaceuticalJun 27, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200mg/mL, CIII, Rx only, 1mL Single-dose vial, Distributed by: Sun
Sun Pharmaceutical recalls 200mg/mL Testosterone Cypionate Injection vials due to water leakage risk. This could affect product safety and efficacy. Consumers should check NDC 62756-015-40 for affected units.
Sun PharmaceuticalJun 21, 2022 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm
Sun Pharmaceutical recalls 20mg esomeprazole capsules due to superpotent drug levels. This may cause serious health effects if taken as prescribed. Consumers should contact the manufacturer for details.
Sun PharmaceuticalJun 21, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun
Sun Pharmaceutical recalls testosterone injections due to potential contamination from a manufacturing issue. Affected lots may pose a risk of infection if used.
Sun PharmaceuticalJun 10, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries
Sun Pharmaceutical recalls 0.125mg Clonazepam orally disintegrating tablets due to oversized tablets found in bottles. This may affect prescription medication safety.
Sun PharmaceuticalJun 3, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun
Sun Pharmaceutical recalls testosterone cypionate injections due to manufacturing impurities that could affect safety. Affected lots have specific NDC and expiration dates. Consumers should contact pharmacy for details.
Sun PharmaceuticalJun 3, 2022 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical
Sun Pharmaceutical recalls specific lots of Testosterone Cypionate Injection due to manufacturing deviations causing abnormal machine parts. Affected lots have expiration dates through November 2022.
Sun PharmaceuticalJun 3, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for:
Sun Pharmaceutical recalls 150 mg/mL medroxyprogesterone acetate injectable syringes (NDC 16714-999-01) due to lack of sterility assurance. Affected lots expired between June 2022 and June 2023. Contact for details.
Sun PharmaceuticalMay 6, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg, 60-count bottle, Rx only Distributed by: Sun
Sun Pharmaceutical recalls 200mg bupropion extended-release tablets due to dark gritty substance from desiccant canister. Affected bottles have NDC 47335-738-86, lot HAC2237A, expiring 05/2023.
Sun PharmaceuticalApr 29, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, packaged in 6 pouches x 10 single-use vials (0.25 mL each) per box,
Sun Pharma recalls Cequa (cyclosporine ophthalmic solution) 0.09% due to subpotent drug levels and particulate matter. Affected units have NDC 47335-506-96, lots 10014/10016, expiring 08/2022. Consumers should contact Sun Pharma for details.
Sun PharmaApr 1, 2022 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Chlorthalidone Tablets USP 25 mg, Rx Only, 100 Tablets, Sun Pharma, Mfg. by: Fontida Bio Pharm Inc., 1100 Orthodox St.
Sun Pharma recalls 25mg Chlorthalidone tablets with stainless steel particles. Foreign matter in tablets may cause injury. Stop using and contact for return.
Sun PharmaFeb 7, 2022 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141,
Sun Pharmaceutical recalls 5mg Tadalafil tablets due to incorrect Crospovidone grade in manufacturing. This may affect safety but does not cause immediate harm. Check NDC #16714-075-01 and lot number DNC1127A.
Sun PharmaceuticalOct 25, 2021 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Pregabalin Capsules, 50 mg, 100 count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury,
Sun Pharmaceutical recalls 696 bottles of Pregabalin 50mg capsules due to failed particle size and bulk density specifications. Check your lot number.
Sun Pharmaceutical IndustriesOct 22, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count blister
Sun Pharmaceutical recalls AllerClear D-24 hr tablets due to failed moisture limits. This may cause reduced effectiveness or safety issues. Check your product for the NDC 63981-724-15 label.
Sun Pharmaceutical IndustriesOct 12, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by:
Sun Pharmaceutical recalls Venlafaxine 50mg tablets due to foreign tablets found in some bottles. Consumers should check product labels and contact Sun Pharmaceutical for details.
Sun Pharmaceutical Industries IncJul 29, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)),
Sun Pharma recalls Cequa (cyclosporine ophthalmic solution) 0.09% vials due to subpotent strength and particulates. This affects patients using the medication for eye conditions. Contact Sun Pharma for details.
Sun PharmaMay 7, 2021 - Stop using nowDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Metformin HCl Extended-Release Tablets, USP, 500 mg, packaged in 500-count bottles, Rx only, Distributed by: Sun
Sun Pharmaceutical recalls 500-count Metformin HCl Extended-Release Tablets (500 mg) due to activated carbon contamination. Affected lots expire 6/2032 or 7/2023. Stop using immediately if you have these specific lots.
Sun PharmaceuticalMay 4, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor, 16 fl. oz., 473 mL bottles Rx Only,
Sun Pharmaceutical recalls Riomet (metformin hydrochloride oral solution) 500mg/5mL Cherry Flavor bottles due to microbial contamination. This poses a risk of infection from non-sterile product. Consumers should check NDC 10631-206-02 and lot numbers listed.
Sun PharmaceuticalMar 31, 2021
SUN PHARMACEUTICAL INDUSTRIES INC recall questions
How many recalls has SUN PHARMACEUTICAL INDUSTRIES INC had?
140 recalls from SUN PHARMACEUTICAL INDUSTRIES INC are on record with U.S. safety agencies, from 2013–2026.
What is the most recent SUN PHARMACEUTICAL INDUSTRIES INC recall?
SUN PHARMACEUTICAL INDUSTRIES INC recalls Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro, dated Sep 25, 2026. Every SUN PHARMACEUTICAL INDUSTRIES INC recall is listed on this page, newest first.
Why are SUN PHARMACEUTICAL INDUSTRIES INC products recalled?
The most common reasons on record: Failed Impurities/Degradation Specifications (10); Failed Dissolution Specifications (7); Lack of assurance of sterility (5); Cross Contamination (2).
What should I do if I have a recalled SUN PHARMACEUTICAL INDUSTRIES INC product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new SUN PHARMACEUTICAL INDUSTRIES INC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.