Drugs & medicalNot Yet Classified

Aurobindo Pharma USA Inc recalls amazon, Acetaminophen, Extra Strength, 500mg Caplets, 1000-count bottle, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N.,…

Discoloration: consumer complaints received for discolored tablets

Read the official notice →
Date
2026-10-07
Country
United States
Brand
Aurobindo Pharma
Product
amazon, Acetaminophen, Extra Strength, 500mg Caplets, 1000-count bottle, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N.,…
Classification
Not Yet Classified
Units
US Nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Aurobindo Pharma recalls

  1. 2026-08-12
  2. US
  3. 2025-06-25
  4. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc recalls Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, NDC…

    cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).

    FDA · DrugAurobindo Pharma USA IncUSA Nationwide.Official notice →
  5. 2024-12-25
  6. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc recalls Nebivolol Tablets, 2.5. mg, 30-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East…

    CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit.

    FDA · DrugAurobindo Pharma USA IncNationwide in the USAOfficial notice →
  7. 2024-12-11
  8. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc recalls Cinacalcet Tablets, 60mg, packaged in: a) 30-count HDPE bottle (NDC 65862-832-30), b) 500-count HDPE bottle (NDC 65862-832-05), Rx Only,…

    cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

    FDA · DrugAurobindo Pharma USA IncUSA NationwideOfficial notice →
  9. 2024-08-28
  10. US
    Drugs & medicalClass I

    Aurobindo Pharma USA Inc recalls Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles, Distributed by:…

    Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.

    FDA · DrugAurobindo Pharma USA IncNJ, NY & PAOfficial notice →
  11. 2024-05-15
  12. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc. recalls Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) 100 tablets per bottle, NDC 13107-283-01, b) 500 tablets per bottle, NDC…

    Discoloration: Dotted and yellow spots on tablets

    FDA · DrugAurobindo Pharma USA Inc.Nationwide in the USAOfficial notice →
All 15 Aurobindo Pharma recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-07
  2. US
  3. US
    Drugs & medicalClass II

    Amneal Pharmaceuticals, LLC recalls Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08907, NDC…

    Defective Container; packets were found to be either empty or partially full.

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide in the USA.Official notice →
  4. US
    Drugs & medicalClass II

    Ajanta Pharma USA Inc recalls Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC:…

    Failed Dissolution Specifications: below specification

    FDA · DrugAjanta Pharma USA IncNationwide in the US.Official notice →
  5. 2026-09-30
  6. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3)…

    The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as…

    FDA · DeviceMedline Industries, LPUS Nationwide.Official notice →
  7. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to…

    There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  8. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02

    Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution.Official notice →
See all drugs & medical recalls →