Drugs & medicalClass II

Teva Pharmaceuticals USA, Inc recalls Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC…

Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin

Read the official notice →
Date
2026-04-29
Country
United States
Brand
Teva Pharmaceuticals
Product
Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC 0555-1054-60;…
Classification
Class II
Units
Nationwide in the USA, Puerto Rico and Virgin Islands
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Teva Pharmaceuticals recalls

  1. 2026-09-09
  2. US
  3. 2026-05-13
  4. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL vial of…

    Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

    FDA · DrugTeva Pharmaceuticals USA, IncNationwide in the USAOfficial notice →
  5. 2026-04-15
  6. US
  7. US
  8. 2026-04-01
  9. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only,…

    Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

    FDA · DrugTeva Pharmaceuticals USA, IncNationwide in the USAOfficial notice →
  10. 2026-03-11
  11. US
All 44 Teva Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2026-04-29
  2. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.

    Software issue that renders the touch screen unresponsive.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)Worldwide - US Nationwide distribution in the states of MI & NY. The countries…Official notice →
  3. US
    Drugs & medicalClass II

    Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The…

    In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.

    FDA · DeviceUvlizer c/o RAIS INTERNATIONAL LLCU.S.Official notice →
  4. US
    Drugs & medicalClass II

    Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission…

    In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.

    FDA · DeviceUvlizer c/o RAIS INTERNATIONAL LLCU.S.Official notice →
  5. US
    Drugs & medicalClass II

    B BRAUN MEDICAL INC recalls DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.

    Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

    FDA · DrugB BRAUN MEDICAL INCUS Nationwide.Official notice →
  6. US
    Drugs & medicalClass II

    The Harvard Drug Group LLC recalls Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and…

    Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.

    FDA · DrugThe Harvard Drug Group LLCNationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Premier Dental Products Co recalls Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Romano Drive,…

    Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the…

    FDA · DrugPremier Dental Products CoNationwide within the United StatesOfficial notice →
See all drugs & medical recalls →