Drugs & medicalClass II

Viatris recalls Lyrica CR (pregabalin) extended release tablets, 330 mg, 30-count bottles, Rx only, Distributed by Parke-Davis Division of Pfizer Inc.,…

Failed Dissolution Specifications

Read the official notice →
Date
2021-10-06
Country
United States
Brand
Viatris
Product
Lyrica CR (pregabalin) extended release tablets, 330 mg, 30-count bottles, Rx only, Distributed by Parke-Davis Division of Pfizer Inc.,…
Classification
Class II
Units
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Viatris recalls

  1. 2023-06-14
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    Viatris Inc recalls Levsin injection (hyoscyamine sulfate injection, USP), 0.5 mg per ml in water for Injection, 1 ml Ampule (Box of 5 ampules), Rx Only,…

    CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.

    FDA · DrugViatris IncProduct was distributed to 10 distributors who may have further distribute the…Official notice →
  3. 2022-11-23
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    Viatris Inc recalls Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC…

    Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.

    FDA · DrugViatris IncNationwide in the USAOfficial notice →
  5. 2022-11-16
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    Viatris Inc recalls Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only,…

    Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.

    FDA · DrugViatris IncNationwide in the USAOfficial notice →
  7. 2022-10-05
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    Viatris Inc recalls Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan…

    Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.

    FDA · DrugViatris IncNationwide in the USAOfficial notice →
  9. 2022-05-18
  10. US
    Drugs & medicalClass II

    Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer…

    Failed Dissolution Specifications: low out of specification results for dissolution.

    FDA · DrugViatris IncProduct was distributed nationwide in the USAOfficial notice →
  11. 2022-05-11
  12. US
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    Viatris Inc recalls alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.

    Failed Dissolution Specifications: low out-of-specification dissolution test results observed.

    FDA · DrugViatris IncProduct was distributed nationwide in the USAOfficial notice →
All 12 Viatris recalls →

Other drugs & medical recalls in the United States

  1. 2021-10-06
  2. US
  3. US
    Drugs & medicalClass II

    American Health Packaging recalls Valproic Acid Oral Solution, USP, 500 mg/10 mL, 100 10 mL unit dose cups per case, Rx Only, Packaged and Distributed by: American…

    CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.

    FDA · DrugAmerican Health PackagingNationwide USAOfficial notice →
  4. US
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    New Vision Pharmaceuticals LLC recalls CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials Mixed Berry Flavor 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06…

    Subpotent Drug

    FDA · DrugNew Vision Pharmaceuticals LLCAL, CA, FL, IN, MI, MO, NJ, NY, PA, RI, SC, TN, TX, VAOfficial notice →
  5. US
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    Johnson & Johnson Consumer, Inc. recalls Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%),…

    Chemical Contamination: presence of benzene

    FDA · DrugJohnson & Johnson Consumer, Inc.Nationwide in USOfficial notice →
  6. US
  7. US
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    Jacobus Pharmaceutical Company Inc. recalls Ruzurgi (amifampridine) Tablets 10 mg, packaged in 100-count bottles, Rx only, Manufactured by: Jacobus Pharmaceutical…

    Microbial contamination of non-sterile products: Firm's testing found lots to exceed specification for aerobic bacteria, yeast, and mold counts.

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See all drugs & medical recalls →