RemedyRePack Inc. recalls
Every recall we track for RemedyRePack Inc. — 61 in all, from 2015–2025 — plus the complaints and injury reports the public filed about them. 3 are rated “stop using now”.
Recalls per year, by danger level
Recalls from RemedyRePack Inc. peaked in 2023 (17); 52 since 2017. 6% rated “stop using now”.
All FDA recall records for RemedyRePack 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 | 1 | 1 | 0 | 2 |
| 2018 | 0 | 0 | 1 | 8 | 9 |
| 2019 | 2 | 0 | 1 | 2 | 5 |
| 2020 | 0 | 0 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 2 | 1 | 3 |
| 2022 | 0 | 1 | 3 | 3 | 7 |
| 2023 | 0 | 0 | 4 | 13 | 17 |
| 2024 | 1 | 0 | 2 | 1 | 4 |
| 2025 | 0 | 1 | 0 | 2 | 3 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
RemedyRePack Inc. recalls before 2017
Recalls on record by year.
Most common reasons for RemedyRePack Inc. recalls
What to do if you have a recalled RemedyRePack 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 RemedyRePack Inc. recalls
36 shown- Use cautionDrug
RemedyRePack Inc. recalls Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRePack Inc. recalls specific lots of Clindamycin HCl Capsules, 300 mg due to current Good Manufacturing Practice deviations in a shared facility.
RemedyRePackApr 22, 2025 - UnratedDrug
RemedyRepack Inc. recalls Clindamycin HCl, 300 mg Capsule, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRepack Inc. recalls 300 mg Clindamycin HCl capsules due to CGMP deviations. Affected lots expire by Dec 2025. Consumers should contact the company for details.
RemedyRepackMar 24, 2025 - UnratedDrug
RemedyRepack Inc. recalls Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ
RemedyRepack recalls Carvedilol 25mg tablets due to unsafe N-Nitroso Carvedilol Impurity-1 levels. Affected lots expire May 2025 and July 2025. Stop using immediately if you have these specific lots.
RemedyRepackJan 24, 2025 - UnratedDrug
RemedyRepack Inc. recalls Duloxetine Delayed-Release Capsules, 60 mg, a) 30 count blister cards (NDC 70518-0937-04), b) 30 count bottles (NDC
RemedyRepack recalls Duloxetine Delayed-Release Capsules 60mg due to N-nitroso-duloxetine impurity exceeding safety limits. Rx-only product sold in blister cards and bottles with specific NDCs.
RemedyRepackDec 2, 2024 - Lower riskDrug
RemedyRepack Inc. recalls Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark,
RemedyRepack recalls Potassium Chloride Micro 10mEq K Extended Release Capsules due to dissolution testing failures. This may affect medication effectiveness. Check NDC 70518-1203-03 and lot numbers for affected products.
RemedyRepackJun 26, 2024 - Stop using nowDrug
RemedyRepack Inc. recalls Phenazopyridine HCl, 100mg tablets, 6 count bottles, Rx Only, Repackaged by: RemedyRepack, Inc., Indiana, PA NDC#:
RemedyRepack recalls 100mg Phenazopyridine tablets that were mistakenly repackaged with Phenobarbital. This mix-up could cause serious harm if taken by mistake.
RemedyRepackMay 31, 2024 - Lower riskDrug
RemedyRepack Inc. recalls TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC
RemedyRepack recalls 30-count and 90-count blister packs of TraMADol HCl 50mg tablets due to potential presence of baclofen tablets. Consumers should check their product details and contact the manufacturer for guidance.
RemedyRepackMay 2, 2024 - UnratedDrug
RemedyRepack Inc. recalls Ketotifen Fumarate 0.025 %, Antihistamine eye drops, 5mL bottle, MFG: Akorn, Lake Forrest IL 60045, Repackaged by:
RemedyRepack Inc. recalls Ketotifen Fumarate 0.025% eye drops due to quality program discontinuation. Affected units may not meet safety standards. Consumers should check NDC and lot numbers for recall.
RemedyRepackMay 1, 2023 - UnratedDrug
RemedyRepack Inc. recalls Simvastatin 10 mg tablets, packaged in a) 30-count bottles (NDC 70518-0064-01) and b) 90-count bottles (NDC
RemedyRepack Inc. recalls Simvastatin 10mg tablets with specific NDC codes due to cGMP deviations. These prescription-only medications may have quality issues affecting safety.
RemedyRepackMar 20, 2023 - Lower riskDrug
RemedyRepack Inc. recalls Rifampin Capsules, 300 mg, 30 count blister card, Rx only, Mfg: Lupin Pharma, Baltimore, MD 21202, original NDC
RemedyRepack Inc. recalls 300 mg Rifampin Capsules due to failed impurities and degradation specifications. This Rx-only medication may pose risks if not used properly.
RemedyRepackDec 20, 2022 - Lower riskDrug
RemedyRepack Inc. recalls Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc.,
RemedyRepack recalls 0.2 mg Desmopressin tablets due to subpotency. Affected products have specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
RemedyRepackDec 5, 2022 - Lower riskDrug
RemedyRepack Inc. recalls Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack
RemedyRepack recalls 10mg Lisinopril tablets with a metal piece in one tablet. Stop using if you have the specific lot numbers listed. No remedy provided in official notice.
RemedyRepackSep 15, 2022 - Use cautionDrug
RemedyRepack Inc. recalls Losartan HCTZ 50/12.5 mg, 90 count bottle Original NDC# 33342-0050-10 Repackaged NDC# 70518-3231-00
RemedyRepack Inc. recalls specific lots of Losartan HCTZ 50/12.5 mg bottles due to CGMP deviations and azido impurity levels above acceptable limits.
RemedyRepack Inc.May 4, 2022 - UnratedDrug
RemedyRepack Inc. recalls Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09
RemedyRePack recalls Losartan HCTZ 100/25 mg tablets due to AZIDO impurity levels above safety limits. Affected lots expired by 10/31/2022.
RemedyRePackMay 2, 2022 - UnratedDrug
RemedyRepack Inc. recalls Losartan Potassium 50 mg Tablet, a) 30-count blister card (NDC# 70518-3282-1), b) 60-count blister card (NDC:
RemedyRePack recalls Losartan Potassium 50mg tablets with AZIDO impurities above safety limits. Stop using if you have these specific blister packs.
RemedyRePackApr 6, 2022 - Lower riskDrug
RemedyRepack Inc. recalls Metformin 750 mg Extended Release NDC # 70518-2920-00
RemedyRePack recalls Metformin 750mg Extended Release tablets with NDMA levels above safe limits. Consumers should check product lot numbers and contact the company for a replacement.
RemedyRePackDec 30, 2021 - UnratedDrug
RemedyRepack Inc. recalls Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC
RemedyRePack recalls Cefixime 400mg capsules with failed impurities/degradation specs. Rx-only products from specific lots and NDCs may pose safety risks.
RemedyRePackDec 29, 2021 - Lower riskDrug
RemedyRepack Inc. recalls Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05,
RemedyRepack Inc. recalls 180-count Carvedilol 25mg bottles (Rx only) that accidentally contain Paroxetine tablets due to repackaging error. This could cause unintended medication interactions.
RemedyRepackAug 17, 2021 - Lower riskDrug
RemedyRepack Inc. recalls Metformin Hydrochloride Extended Release 750 mg, 30 count blister cards, Rx only, Repackaged by: RemedyRepack Inc.,
RemedyRepack recalls Metformin Hydrochloride Extended Release 750mg blister packs due to detected N-Nitrosodimethylamine (NDMA) impurity above safe levels. This may pose health risks with long-term use.
RemedyRepackOct 11, 2020 - Lower riskDrug
RemedyRepack Inc. recalls Carbamazepine 200 mg Tablets, 100-unit dose tablets per box, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRePack recalls 200mg Carbamazepine tablets with failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
RemedyRePackJun 29, 2020 - Stop using nowDrug
RemedyRepack Inc. recalls Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRePack recalls Ketorolac Trom injections due to small black particles found during visual inspection. Affected products have specific NDC and lot numbers. Stop using immediately.
RemedyRePackDec 27, 2019 - Stop using nowDrug
RemedyRepack Inc. recalls Ranitidine 150 mg tablet Original Supplier's NDC 65162-0253-10 Remedy Repackaged NDC 70518-1714-00
RemedyRePack recalls Ranitidine 150mg tablets with potential NDMA levels above safety limits. Consumers should check lot numbers and contact the company for details.
RemedyRePackDec 11, 2019 - Lower riskDrug
RemedyRepack Inc. recalls Lisinopril/HCTZ 20mg/12.5mg Tablet, QTY: 30 tablets per blister card, MFG: Lupin Pharma Baltimore, MD 21202, NDC
RemedyRePack recalls 30-tablet blister packs of Lisinopril/HCTZ 20mg/12.5mg due to foreign tablets found in some bottles. Affected lots from 2019-09-30 expiry.
RemedyRePackAug 5, 2019 - UnratedDrug
RemedyRepack Inc. recalls Losartan Potassium/HCTZ, 100 mg/12.5 mg Tablet, 90-Count bottle, Manufactured by Torrent Pharmaceuticals, Distributed
FDA-confirmed impurity in Losartan Potassium/HCTZ tablets may exceed safe levels. Recalled batch: NDC 70518-1560-00, Lot B05170:101618, expiring 10/2019. Consumers should contact manufacturer for details.
RemedyRepackApr 22, 2019 - UnratedDrug
RemedyRepack Inc. recalls Losartan 50mg Tablet, 30 count each blister card.
RemedyRePack recalls Losartan 50mg tablets due to trace impurities detected in manufacturing. Affected lots may pose health risks; contact for return instructions.
RemedyRePackMar 14, 2019 - Lower riskDrug
RemedyRepack Inc. recalls Nitrofurantoin Monohydrate/Macrocrystals capsules,100 mg, packaged in HDPE 60 cc bottles, Rx only, MFG: Sandoz Inc.,
RemedyRepack recalls Nitrofurantoin 100mg capsules due to potential cross contamination with unrelated drugs like Benazepril and Haloperidol. Consumers should contact the company for details.
RemedyRepackNov 7, 2018 - UnratedDrug
RemedyRepack Inc. recalls Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902,
RemedyRePack recalls Metoprolol Tartrate Injection vials due to pH instability. This may affect medication safety. Check your vial lot numbers for affected batches.
RemedyRePackOct 26, 2018 - UnratedDrug
RemedyRepack Inc. recalls Amlodipine/Valsartan HCTZ 10 mg/320 mg/25 mg tablets, HDPE 90 cc bottles in cardboard trays Original NDC 13668-0325-30
RemedyRePack recalls 10 mg/320 mg/25 mg Amlodipine/Valsartan HCTZ tablets in HDPE bottles due to trace NDMA impurity detected in manufacturing.
RemedyRePackAug 24, 2018 - UnratedDrug
RemedyRepack Inc. recalls Amlodipine/Valsartan/HCTZ 10mg/320mg/25mg Tablet, Rx Only (HDPE 90cc Bottles in cardboard trays) MFG Torrent Pharma
RemedyRePack recalls 10mg/320mg/25mg Amlodipine/Valsartan/HCTZ tablets (Rx only) due to trace NDMA impurity detected in manufacturing. Consumers should contact the company for details.
RemedyRePackAug 20, 2018 - UnratedDrug
RemedyRepack Inc. recalls Valsartan 160 mg Tablets, HDPE 90 cc bottles in cardboard trays, Rx Only, RemedyRepack, Inc., 625 Kolter Drive, Suite
RemedyRepack recalls Valsartan 160mg tablets with potential carcinogen impurity in the manufacturing process. Affected lots have specific expiration dates and NDC numbers. Consumers should contact the manufacturer for details.
RemedyRepackAug 10, 2018 - UnratedDrug
RemedyRepack Inc. recalls Valsartan/HCTZ 320mg/12.5 mg tablet, 90-count bottle, Rx only, RemedyRepack, 625 Kolter Drive, Suite 4, Indiana, PA
RemedyRepack recalls 320mg/12.5mg Valsartan/HCT: Carcinogen impurity detected in manufacturing. Rx-only tablets with lot # B0383153-122917. Contact for return instructions.
RemedyRepackJul 17, 2018 - Use cautionDrug
RemedyRepack Inc. recalls Ketorolac Trom 30 mg/mL Injection, packaged in a) 1 mL vials, NDC 61786-0741-01 (Orig: 00548-9021-00), Ref: 33631 and
RemedyRepack recalls Ketorolac 30 mg/mL injections with visible crystalline particles that could cause serious injury if injected.
RemedyRepackAug 22, 2017 - Lower riskDrug
RemedyRepack Inc. recalls Glipizide 2.5 mg ER Tablets, Manufactured by Watson Laboratories, Inc., Parsippany, NJ 07054, Repackaged by
RemedyRepack recalls Glipizide 2.5mg ER tablets with failed dissolution specifications. These tablets may not release medication properly, risking ineffective treatment. Contact for return instructions.
RemedyRepackFeb 7, 2017 - Use cautionDrug
RemedyRepack Inc. recalls Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by:
RemedyRepack Inc. recalls Bicillin L-A syringes due to incorrect storage instructions on the label. Check lot numbers and expiration dates.
BicillinNov 11, 2015 - Use cautionDrug
RemedyRepack Inc. recalls KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by
RemedyRepack Inc. recalls specific lots of Ketorolac Tromethamine injection due to crystallization. Check lot numbers and expiration dates immediately.
RemedyRepackApr 23, 2015 - Use cautionDrug
RemedyRepack Inc. recalls KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by
RemedyRepack Inc. recalls specific lots of Ketorolac Tromethamine injection due to crystallization. Check lot numbers and expiration dates for affected vials.
RemedyRepackFeb 18, 2015
RemedyRePack Inc. recall questions
How many recalls has RemedyRePack Inc. had?
61 recalls from RemedyRePack Inc. are on record with U.S. safety agencies, from 2015–2025.
What is the most recent RemedyRePack Inc. recall?
RemedyRePack Inc. recalls Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA, dated Apr 22, 2025. Every RemedyRePack Inc. recall is listed on this page, newest first.
Why are RemedyRePack Inc. products recalled?
The most common reasons on record: cGMP Deviations (14); CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits. (3); Crystallization (2).
What should I do if I have a recalled RemedyRePack 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 RemedyRePack 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.