Drugs & medicalClass III

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, NDC…

Cross Contamination

Read the official notice →
Date
2025-04-16
Country
United States
Brand
Sun Pharmaceutical Industries
Product
Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-139-05; b) 1000-count bottles, NDC 62756-139-04;…
Classification
Class III
Units
Nationwide in the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Sun Pharmaceutical Industries recalls

  1. 2025-09-24
  2. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Kit for the Preparation of Technetium Tc 99m Mertiatide, Rx Only, Manufactured by: Sun Pharmaceutical Industries, Inc.…

    Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCUS Nationwide.Official notice →
  3. 2025-08-13
  4. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida BioPharm, Inc., 1100 Orthodox St,…

    Presence of foreign substance: identified as aluminum.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCUSA NationwideOfficial notice →
  5. 2025-07-23
  6. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles, Rx only, Manufactured by: OHM Laboratories, New…

    Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25¿C, 60%RH).

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCRecalled units were distributed to 17 distributors who may have further…Official notice →
  7. 2025-03-12
  8. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New…

    Failed Dissolution Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide within in the USA.Official notice →
  9. 2024-07-24
  10. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Nitrofurantoin Capsules, USP (Macrocrystals), 100 mg, Rx Only, 100 capsules per bottle, Manufactured by: Sidmak Laboratories…

    Failed Dissolution Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USA and Puerto ricoOfficial notice →
  11. 2024-07-10
  12. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Decitabine for Injection 50mg per vial, For intravenous infusion only Cytotoxic Agent, Sterile, Rx Only, Single-Dose Vial,…

    CGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
All 57 Sun Pharmaceutical Industries recalls →

Other drugs & medical recalls in the United States

  1. 2025-04-16
  2. US
    Drugs & medicalClass II

    B. Braun Medical Inc recalls 0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical, Inc.,…

    Presence of Particulate Matter

    FDA · DrugB. Braun Medical IncProduct was distributed to 12 distributors who may have further distributed…Official notice →
  3. US
  4. US
    Drugs & medicalClass II

    ASEGUA THERAPEUTICS LLC recalls Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2x14 blister cards, Rx Only, Manufactured for: Asegua Therapeutics LLC an…

    Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.

    FDA · DrugASEGUA THERAPEUTICS LLCUS NationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Zydus Pharmaceuticals (USA) Inc recalls Venlafaxine Tablets, USP, 75 mg, 100 Tablets, Rx only, Mfg. by: Zydus Lifesciences Ltd, Ahmedabad, India, Dist. by: Zydus…

    Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet.

    FDA · DrugZydus Pharmaceuticals (USA) IncUS Nationwide.Official notice →
  6. 2025-04-10
  7. US
    Drugs & medical

    Kramer Laboratories Recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu Blister Packs Due to Risk of Child Poisoning; Violation of Federal Regulation for…

    The Safetussin over-the-counter cold medicine contains acetaminophen, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the products is not child-resistant…

    CPSCAbout 14,250Official notice →
  8. 2025-04-09
  9. US
    Drugs & medicalClass II

    Beckman Coulter Inc. recalls DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC…

    Beckman Coulter has determined that device software versions V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3. have a defect due of which, when all constituent tests of a calculated result are rerun, either manually ordered by the…

    FDA · DeviceBeckman Coulter Inc.Worldwide Distribution: U.S. (nationwide) to states of: AL, CA, CO, GA, ID,…Official notice →
See all drugs & medical recalls →