Dr. Reddy's Laboratories, Inc. recalls
Every recall we track for Dr. Reddy's Laboratories, Inc. — 163 in all, from 2012–2025 — plus the complaints and injury reports the public filed about them. 11 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Dr. Reddy's Laboratories, Inc. fell by more than half in 2025 (4, down from 20 in 2024). 7% rated “stop using now”.
All FDA recall records for Dr. Reddy's Laboratories, 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 | 0 | 0 | 6 | 7 | 13 |
| 2018 | 0 | 0 | 9 | 8 | 17 |
| 2019 | 9 | 0 | 4 | 10 | 23 |
| 2020 | 0 | 1 | 1 | 0 | 2 |
| 2021 | 0 | 0 | 16 | 5 | 21 |
| 2022 | 0 | 2 | 19 | 1 | 22 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 0 | 11 | 9 | 20 |
| 2025 | 0 | 0 | 4 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Dr. Reddy's Laboratories, Inc. recalls before 2017
Recalls on record by year.
Most common reasons for Dr. Reddy's Laboratories, Inc. recalls
What to do if you have a recalled Dr. Reddy's Laboratories, 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 Dr. Reddy's Laboratories, Inc. recalls
60 shown- Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in
Dr. Reddy's recalls 1mg Varenicline tablets due to subpotent drug levels found in a specific lot during stability testing. This may affect prescription medication efficacy.
Dr. Reddy'sNov 11, 2025 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials, For Intravenous or
Dr. Reddy's recalls 25 vials of Succinylcholine Chloride Injection due to decreased preservative concentration found during stability testing. This may affect medication safety.
Dr. Reddy'sSep 26, 2025 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only, Manufactured by: Dr. Reddy's Laboratories
Dr. Reddy's recalls 20mg omeprazole capsules with foreign Divalproex Sodium tablets. Consumers should check NDC 82009-022-10 and lot C2403017 for affected products.
Dr. Reddy'sJun 30, 2025 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland
Dr. Reddy's recalls Levetiracetam 0.75% Sodium Chloride Injection due to incorrect labeling that could lead to wrong medication use. Affected units have specific NDC and lot numbers.
Dr. Reddy'sMar 13, 2025 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Javygtor (sapropterin dihydrochloride) Tablets 100mg, 120-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories
Dr. Reddy's recalls 100mg Javygtor tablets due to failed impurities/degradation. Affected lots expire by 08/31/2025. Stop using if you have these specific lots.
Dr. Reddy'sNov 22, 2024 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ
Dr. Reddy's recalls 600mg ibuprofen tablets (500-count, Rx only) due to failed tablet specifications. Affected lots made in India, expiring March 2028. Consumers should contact for details.
Dr. Reddy'sOct 29, 2024 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma,
Dr. Reddy's recalls 15mg Morphine Sulfate Extended-Release Tablets due to failed impurities specification. Rx-only product manufactured by Mayne Pharma. No remedy specified in official notice.
Dr. Reddy'sOct 22, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Cinacalcet Tablets, 90 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India.,
Dr. Reddy's recalls 90mg Cinacalcet tablets with potential N-nitroso impurity above FDA limits. Rx-only medication may pose health risks. Check NDC 43598-369-30 and lot numbers for affected batches.
Dr. Reddy'sOct 9, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in
Dr. Reddy's recalls 800mg ibuprofen tablets (Rx only) due to impurities exceeding safety limits. Consumers should check NDC codes and expiration dates for affected lots.
Dr. Reddy'sAug 6, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container, Distributor: Dr. Reddy's
Dr. Reddy's recalls Sevel: 0.8g oral suspension packets with missing lot and expiration dates. Consumers should check labels for correct dates to avoid potential safety issues.
Dr. Reddy'sJun 26, 2024 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC,
Dr. Reddy's Laboratories recalls 300mg allopurinol tablets for foreign substance presence. Rx-only medication with NDC 55111-730-01. No remedy specified in official notice.
Dr. Reddy'sJun 7, 2024 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Eszopiclone Tablets, USP 1mg CIV, 30-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally - 500
Dr. Reddy's recalls 1mg Eszopiclone tablets due to potential impurities. Affected lots: C2302598, expiring 2/29/2025. No specific remedy stated in recall notice.
Dr. Reddy'sJun 4, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's
Dr. Reddy's recalls Zoledronic Acid 5mg/100mL vials due to leaking, risking contamination. Affected lots: G3000010, expiring 11/2025. Contact for details.
Dr. Reddy'sMay 23, 2024 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ
Dr. Reddy's recalls 100-count Sirolimus 1mg tablets (NDC 55111-653-01) due to failed impurities and degradation. Rx-only tablets distributed in the US from India. No specific remedy stated in recall.
Dr. Reddy'sMay 1, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr.
Dr. Reddy's recalls 100mg Sapropterin Dihydrochloride Powder for Oral Solution due to potential decreased potency from discoloration. Affected units have specific lot numbers and expiration dates.
Dr. Reddy'sApr 8, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409
Dr. Reddy's recalls 1mg Glimepiride tablets due to potential misprint on labels. This could lead to incorrect dosing. Affected products have specific NDC and lot numbers. Contact for remedy details.
Dr. Reddy'sJan 18, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409
Dr. Reddy's recalls 4mg tizanidine tablets with foreign 2mg tablets. Consumers should check NDC 55111-180-15 and lot T2304007 for affected products.
Dr. Reddy'sJan 2, 2024 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tacrolimus Capsules, USP 1mg, 100-Count Bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited,
Dr. Reddy's recalls 100-count Tacrolimus capsules (1mg) due to foreign tablets found in some bottles. This is a medication for immunosuppression.
Dr. Reddy'sDec 15, 2023 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Montelukast Sodium Tablets, USP 10 mg, Rx Only, 1000 count bottle, Distributed by: Dr. Reddy's Laboratories.,
Dr. Reddy's recalls 1000-count Montelukast Sodium Tablets due to foreign metoprolol tablets found in some bottles. Consumers should check product details and contact the company for guidance.
Dr. Reddy'sOct 13, 2023 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tacrolimus Capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Mfd. by Dr. Reddy's Laboratories Limited, Bachupally - 500
Dr. Reddy's recalls 0.5mg Tacrolimus capsules due to foreign 1mg capsules in some bottles. This may cause incorrect dosing. Check your bottle's lot number and contact for details.
Dr. Reddy'sFeb 8, 2023 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release
Dr. Reddy's recalls Allergy Relief D tablets that may not dissolve properly, potentially affecting medication effectiveness. This recall covers specific lot numbers and packaging sizes sold through Walmart.
Dr. Reddy'sNov 21, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Phytonadione Injectable Emulsion USP, 10 mg/mL, 25x 1 mL single dose ampules per carton, Rx only, Distributed by: Dr.
Dr. Reddy's recalls 10 mg/mL Phytonadione Injectable Emulsion due to stability issues at 12-month testing. This may affect medication safety. Check NDC 43598-405-16 and lot numbers for affected products.
Dr. Reddy'sSep 14, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10
Dr. Reddy's recalls 15mg Lansoprazole Delayed-Release tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details and contact the manufacturer for instructions.
Dr. Reddy'sJul 13, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 10 Packs of 10 Tablets each, 100 Tablets per blister
Dr. Reddy's recalls 30mg Lansoprazole tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details and contact the manufacturer for guidance.
Dr. Reddy'sApr 15, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories
Dr. Reddy's recalls 30mg Lansoprazole capsules due to failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
Dr. Reddy'sMar 23, 2022 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd. By: Dr. Reddy's Laboratories Limited, Srikakulam -
Dr. Reddy's recalls 80mg Atorvastatin Calcium tablets with impurities that could cause harm. Affected lots from India, expiring 2022-2023. Stop using and contact for details.
Dr. Reddy'sMar 16, 2022 - Use cautionDrug
Dr. Reddy's Laboratories, Inc. recalls Sapropterin Dihydrochloride Powder for Oral Solution, 100 mg, 30 individual packets per carton, Rx Only, Dr. Reddy's,
Dr. Reddy's recalls specific lots of Sapropterin Dihydrochloride Powder for Oral Solution because the drug may be subpotent and out of specification.
Dr. Reddy'sFeb 17, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Azacitidine, 1,00mg/Vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530
Dr. Reddy's recalls certain Azacitidine vials due to failed stability specifications. This may affect drug effectiveness and safety. Check NDC 43598-305-62 and specific lot numbers for affected products.
Dr. Reddy'sJan 19, 2022 - Use cautionDrug
Dr. Reddy's Laboratories, Inc. recalls Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into
Dr. Reddy's recalls Mucus Relief D tablets due to subpotent drug issues. Check lot numbers AT2102065A/B and expiration date 04/2023.
Mucus Relief DJan 10, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets, USP, Allergy &
Dr. Reddy's QC QUALITY CHOICE extended-release allergy tablets with failed dissolution specifications are recalled. Consumers should check NDC 63868-729-10 and lot numbers 79C002624D/79C002625C.
Dr. Reddy'sJan 4, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls 12 HR Allergy & Congestion Relief Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg Antihistamine I Nasal
Dr. Reddy's recalls 12HR allergy relief tablets with failed dissolution specifications. Consumers should check NDC 70000-0518-1 and lot AC2103329G for affected units.
Dr. Reddy'sNov 12, 2021 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC
Dr. Reddy's Ezetimibe and Simvastatin 10mg/40mg tablets (30 or 90 count) recalled due to excipient conductivity issues. Rx-only product with NDC codes 43598-743-30 and 43598-743-90. No remedy specified in official recall.
Dr. Reddy'sOct 5, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules
Dr. Reddy's recalls 20 mg omeprazole capsules due to customer complaints about staples found inside bottles. Affected units contain a staple co-mingled with capsules.
Dr. Reddy'sOct 5, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikakulam
Dr. Reddy's recalls 4mg Tizanidine tablets due to shaved tablets that may cause improper dosing. Affected lots from India, expiring 09/2023.
Dr. Reddy'sJul 19, 2021 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, USP 10 mg, 500-count bottles, Rx Only, Dr. Reddy's Mfd. By: Dr. Reddy's Laboratories
Dr. Reddy's recalls 10mg Atorvastatin tablets due to impurities that could affect safety. Affected lots from 2021 with specific NDC numbers. Consumers should contact the manufacturer for details.
Dr. Reddy'sJun 4, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, USP 10 mg*, Rx Only, 500 count bottle, Mfd By: Dr. Reddy's Laboratories Limited,
Dr. Reddy's recalls 10mg Atorvastatin tablets due to impurities that may affect drug safety. Learn if your product is affected and what to do.
Dr. Reddy'sMay 4, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Progesterone Capsules, 200 mg, 100-count bottles, Rx Only, MADE IN FRANCE; Distributed by: Dr. Reddy's Laboratories,
Dr. Reddy's recalls 200mg progesterone capsules (100-count) made in France due to dissolution testing failures. Rx-only product with batch #1399851P1.
Dr. Reddy'sFeb 26, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40mg, packaged in a) 90-count bottles, NDC 55111-123-90; b) 500-count bottles, NDC
Dr. Reddy's recalls 40mg Atorvastatin Calcium Tablets due to impurities that could pose health risks. Affected products include 90-count and 500-count bottles with specific NDC numbers. Consumers should check labels and contact the manufacturer for details.
Dr. Reddy'sFeb 19, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Imatinib Mesylate Tablets 100mg, packaged as a) 90-count bottles (NDC 43598-344-90); and b) For Institutional Use Only
Dr. Reddy's recalls 100mg Imatinib Mesylate tablets with failed dissolution specs. These tablets may not dissolve properly, affecting drug effectiveness. Contact for return instructions.
Dr. Reddy'sFeb 17, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Esomeprazole Magnesium Delayed Release Capsules USP, 40 mg*, 1000-count bottles, Rx only, Mfd. By: Dr. Reddy's
Dr. Reddy's recalls 40mg esomeprazole capsules with brown pellets. No immediate risk but discoloration may indicate quality issues.
Dr. Reddy'sApr 24, 2020 - Use cautionDrug
Dr. Reddy's Laboratories, Inc. recalls Phytonadione Injectable Emulsion, USP, 10 mg/mL 1 mL ampule (NDC 43598-405-11) packaged in 25 x 1 mL Single-Dose
Dr. Reddy's recalls 25-pack of Phytonadione Injectable Emulsion ampules that may shatter when opened, posing a risk of injury. This medication is prescription-only and distributed by Dr. Reddy's Laboratories.
Dr. Reddy'sMar 16, 2020 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.)
Dr. Reddy's recalls 150mg ranitidine tablets with NDMA impurity detected. Stop using affected batches to avoid potential health risks.
Dr. Reddy'sOct 1, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Divalproex Sodium Extended-Release Tablets, USP, 250 mg a) 100-count bottle (NDC 55111-0533-01), b) 500-count bottle
Dr. Reddy's recalls 250mg Divalproex Sodium Extended-Release Tablets due to packaging humidity exposure. These tablets may degrade in high humidity, affecting safety.
Dr. Reddy'sApr 11, 2019 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Docetaxel Injection USP, 80 mg/4 mL, (20 mg/mL), One-Vial Formulation, Rx only, Mfd By: Dr. Reddy's Laboratories
Dr. Reddy's recalls Docetaxel Injection due to defective container seals that may compromise sterility. Check lot H7081, exp 07/2019.
Dr. Reddy'sMar 6, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC 43598-510-90) b) 1000 count bottle
Dr. Reddy's recalls 40mg esomeprazole capsules with brown pellets. Discoloration may indicate unsafe product. Check NDC codes for affected lots.
Dr. Reddy'sFeb 6, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laboratories
Dr. Reddy's recalls 250mg Divalproex Sodium Extended-release Tablets due to failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
Dr. Reddy'sJan 31, 2019 - Stop using nowDrug
Dr. Reddy's Laboratories, Inc. recalls Ezetimibe and Simvastatin Tablets 10mg/80 mg, 1000-count bottles, Rx only, Manufactured by: Teva Pharmaceuticals Ind.
Dr. Reddy's recalls 1000-count Ezetimibe and Simvastatin tablets with black speckles. Consumers should check NDC 43598-586-10 and lot numbers 43E021/43E023 for affected products.
Dr. Reddy'sJan 15, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's
Dr. Reddy's recalls 300 mg Clopidogrel tablets due to failed dissolution testing at 18 months. Affected lots may not release medication properly.
Dr. Reddy'sDec 10, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's
Dr. Reddy's recalls 300 mg Clopidogrel tablets with failed dissolution testing at 18 months. This could affect medication effectiveness. Consumers should contact the manufacturer for details.
Dr. Reddy'sNov 7, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Levetiracetam in 0.54 % Sodium Chloride Injection 1,500/mg/100mL (15mg/mL), For intravenous Infusion Only, 1 x 100 mL
Dr. Reddy's recalls Levetiracetam injection due to label error showing incorrect strength. The product may be mislabeled as 0.75% Sodium Chloride (1000 mg/100 mL) when it's actually 0.54% Sodium Chloride (1500 mg/100 mL).
Dr. Reddy'sOct 26, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Nystatin and Triamcinolone Acetonide Cream, USP, 100,000 units/gm & 1 mg/gm, packaged in a) 15 g tube (NDC
Dr. Reddy's recalls Nystatin and Triamcinolone Acetonide Cream due to stability issues. Out of specification composition found during testing. Rx only products with specific lot numbers and expiration dates.
Dr. Reddy'sSep 21, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Zoledronic Acid Injection, 5 mg/100 mL (0.05 mg/mL) One 100ml Single-Dose Bottle, Rx Only. NOVAPLUS Mfd By: Gland
Dr. Reddy's recalls Zoledronic Acid Injection due to failed impurities testing. This medication may contain harmful substances that could cause health issues. Affected units have specific batch numbers and expiration dates.
Dr. Reddy'sSep 12, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited Srilakulam - 532
Dr. Reddy's recalls 2mg Tizanidine HCl tablets due to glimepiride tablets found in some bottles. This could cause unintended medication effects. Contact for return instructions.
Dr. Reddy'sSep 4, 2018 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium tablets, 40 mg, 500-count bottle, Rx only, Mfd By: Dr. Reddy's Laboratories Limited, Srikakulam -
Dr. Reddy's recalls 40mg Atorvastatin Calcium tablets (500-count) due to impurity issues detected at 18 months. Consumers should check NDC 55111-123-05 for affected products.
Dr. Reddy'sAug 2, 2018 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC
Dr. Reddy's recalls 40mg Atorvastatin Calcium tablets due to failed impurities and degradation. Rx-only bottles with specific NDCs and lots may be affected. Consumers should contact the manufacturer for details.
Dr. Reddy'sJun 12, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam
Dr. Reddy's recalls 80mg Atorvastatin tablets due to foreign objects in some bottles. Consumers should check NDC 55111-124-90 for affected lots. No remedy specified in official notice.
Dr. Reddy'sMay 30, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's
Dr. Reddy's recalls 100-mg Metoprolol Succinate Extended-Release Tablets due to foreign Clopidogrel tablets found in some bottles. This is a prescription-only product.
Dr. Reddy'sApr 23, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ
Dr. Reddy's recalls 0.1% Clocortolone Pivalate Cream tubes due to stability testing failures. This cream may not be effective or safe after expiration.
Dr. Reddy'sMar 8, 2018 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets 10 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories,
Dr. Reddy's recalls 10mg Atorvastatin Calcium tablets with impurities detected. Affected lots from March 2018 and May 2018. Stop using if you have these specific bottles.
Dr. Reddy'sJan 29, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube,
Dr. Reddy's recalls Doan's Pain Relieving Cream with missing lot/exp dates causing product mix-ups. Consumers should check labels for correct dates to avoid confusion.
Dr. Reddy'sOct 30, 2017
Dr. Reddy's Laboratories, Inc. recall questions
How many recalls has Dr. Reddy's Laboratories, Inc. had?
163 recalls from Dr. Reddy's Laboratories, Inc. are on record with U.S. safety agencies, from 2012–2025.
What is the most recent Dr. Reddy's Laboratories, Inc. recall?
Dr. Reddy's Laboratories, Inc. recalls Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in, dated Nov 11, 2025. Every Dr. Reddy's Laboratories, Inc. recall is listed on this page, newest first.
Why are Dr. Reddy's Laboratories, Inc. products recalled?
The most common reasons on record: CGMP Deviations: Presence of NDMA impurity detected in product. (18); Failed Dissolution Specifications (13); Failed dissolution specifications (10); Subpotent Drug: Subpotent atorvastatin. (7).
What should I do if I have a recalled Dr. Reddy's Laboratories, 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 Dr. Reddy's Laboratories, 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.