Drugs & medicalClass II

Amneal Pharmaceuticals, LLC recalls chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100-count bottles Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral…

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Read the official notice →
Date
2025-09-10
Country
United States
Brand
Amneal Pharmaceuticals
Product
chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100-count bottles Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral…
Classification
Class II
Units
Distributed 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Amneal Pharmaceuticals recalls

  1. 2026-06-17
  2. US
    Drugs & medicalClass III

    Amneal Pharmaceuticals, LLC recalls Primidone Tablets, USP, 50 mg, 100 Tablets per Bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage…

    Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide within the USA.Official notice →
  3. 2026-04-08
  4. US
    Drugs & medicalClass I

    Amneal Pharmaceuticals, LLC recalls Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only,…

    Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

    FDA · DrugAmneal Pharmaceuticals, LLCU.S.A. NationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Amneal Pharmaceuticals, LLC recalls traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad…

    Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during Long term stability (25¿C/60%RH).

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide within the USAOfficial notice →
  6. 2025-06-18
  7. US
    Drugs & medicalClass I

    Amneal Pharmaceuticals, LLC recalls Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, Rx Only, a) 100 Tablets per Bottle, NDC: 65162-271-10, b) 500 Tablets…

    Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination.

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide in the USAOfficial notice →
  8. 2025-05-14
  9. US
  10. 2024-08-14
  11. US
    Drugs & medicalClass III

    Amneal Pharmaceuticals, LLC recalls Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC#…

    Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide in the USAOfficial notice →
All 8 Amneal Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2025-09-10
  2. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

    Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP…

    FDA · DeviceBaxter Healthcare CorporationUS distribution including Puerto Rico and OUS (International) CanadaOfficial notice →
  3. US
  4. US
  5. US
  6. US
    Drugs & medicalClass I

    DermaRite Industries, LLC recalls PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side…

    Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

    FDA · DrugDermaRite Industries, LLCNationwide within the USAOfficial notice →
  7. US
    Drugs & medicalClass II

    Boothwyn Pharmacy LLC recalls Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy

    Subpotent Drug

    FDA · DrugBoothwyn Pharmacy LLCU.S. NationwideOfficial notice →
See all drugs & medical recalls →