Drugs & medicalClass II

Teva Pharmaceuticals USA, Inc recalls Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales, PA 19454,…

Superpotent Drug

Read the official notice →
Date
2024-08-28
Country
United States
Brand
Teva Pharmaceuticals
Product
Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales, PA 19454, NDC…
Classification
Class II
Units
Product was distributed nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-11-05
  2. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Prazosin Hydrochloride, Capsules, USP, 2 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100…

    CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.

    FDA · DrugTeva Pharmaceuticals USA, IncU.S. NationwideOfficial notice →
  3. 2025-07-02
  4. US
  5. 2025-02-12
  6. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC…

    Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit

    FDA · DrugTeva Pharmaceuticals USA, IncProduct was distributed nationwide.Official notice →
  7. 2024-07-24
  8. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Fludrocortisone Acetate Tablets, USP 0.1mg, Rx Only, 100 Tablets per bottle, Manufactured in Canada By: Patheon, Inc.,…

    Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.

    FDA · DrugTeva Pharmaceuticals USA, IncNationwide in the USA and Puerto RicoOfficial notice →
  9. 2024-06-26
  10. US
  11. 2024-04-17
  12. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc.,…

    Superpotent Drug: The 3-month stability result for assay was found to be above specification limit

    FDA · DrugTeva Pharmaceuticals USA, IncNationwide in the USAOfficial notice →
All 44 Teva Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2024-08-28
  2. 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 →
  3. US
    Drugs & medicalClass II

    Zeco LLC recalls Rubbing Alcohol (70% Isopropyl Alcohol), First-Aid Antiseptic, packaged in a) 3.78L (1-gallon jug); and b) 208.19L (55-gallon drum), Sold…

    CGMP Deviations: sterile water not used for production

    FDA · DrugZeco LLCNationwide within the United States and Toronto, Canada (Rubbing alcohol)Official notice →
  4. US
  5. US
  6. US
    Drugs & medicalClass I

    Hikma Pharmaceuticals USA Inc. recalls Acetaminophen Injection, 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose bags, For Intravenous Use Only, Rx Only, Manufactured…

    Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL)

    FDA · DrugHikma Pharmaceuticals USA Inc.OH and PROfficial notice →
  7. 2024-08-21
  8. US
    Drugs & medicalClass II

    Argon Medical Devices, Inc recalls L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539

    Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.

    FDA · DeviceArgon Medical Devices, IncUS distribution to the states of: TX, WA, CA, ILOfficial notice →
See all drugs & medical recalls →