Drugs & medicalClass II

Amerisource Health Services LLC recalls Carbamazepine Extended-Release Tablets, USP 400 mg, 30 Tablets per carton (3x10 unit dose cards), Rx Only, American Health…

Failed Dissolution Specifications.

Read the official notice →
Date
2025-10-08
Country
United States
Brand
Amerisource Health Services
Product
Carbamazepine Extended-Release Tablets, USP 400 mg, 30 Tablets per carton (3x10 unit dose cards), Rx Only, American Health Packaging,…
Classification
Class II
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Amerisource Health Services recalls

  1. 2026-02-18
  2. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product…

    Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

    FDA · DrugAmerisource Health Services LLCNationwide in the USAOfficial notice →
  3. 2025-11-05
  4. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Prazosin Hydrochloride, Capsules, USP, 5 mg, 20 capsules (5x4) cartons, Rx only, Distributed by American Health Packaging,…

    Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit

    FDA · DrugAmerisource Health Services LLCNationwide within the United StatesOfficial notice →
  5. 2025-10-22
  6. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217,…

    CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity…

    FDA · DrugAmerisource Health Services LLCNationwide within the United StatesOfficial notice →
  7. 2025-09-24
  8. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100 (10x10) blisterpack per carton, Rx Only, Distributed by: American Health…

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

    FDA · DrugAmerisource Health Services LLCNationwide in the USAOfficial notice →
  9. 2025-09-03
  10. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217…

    CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity…

    FDA · DrugAmerisource Health Services LLCNationwideOfficial notice →
  11. 2025-06-11
  12. US
All 31 Amerisource Health Services recalls →

Other drugs & medical recalls in the United States

  1. 2025-10-08
  2. US
    Drugs & medicalClass II

    Getinge Disinfection Ab recalls Getinge 88-Series Washer- Disinfector. Model Number: 88-5.

    Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.

    FDA · DeviceGetinge Disinfection AbWorldwide - US Nationwide distribution in the states of Colorado,…Official notice →
  3. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842,…

    The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages…

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice →
  4. US
    Drugs & medicalClass II

    Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%, a) 5 mL and b) 10 mL, Rx Only, Sterile, Manufactured by: Apotex Inc.,…

    Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns

    FDA · DrugApotex Corp.Nationwide in the USOfficial notice →
  5. US
    Drugs & medicalClass II

    Zydus Pharmaceuticals (USA) Inc recalls Entecavir Tablets, USP, 0.5 mg, 30-count bottle, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India,…

    Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity

    FDA · DrugZydus Pharmaceuticals (USA) IncDistributed Nationwide in the USAOfficial notice →
  6. 2025-10-01
  7. US
    Drugs & medicalClass II

    Maquet Cardiovascular, LLC recalls Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH)…

    Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft,…

    FDA · DeviceMaquet Cardiovascular, LLCUS Nationwide distribution in the states of FL, IL, MD & TX.Official notice →
  8. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers: K102005, K130842, K130638,…

    Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system…

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice →
See all drugs & medical recalls →