Drugs & medicalClass II

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.

Read the official notice →
Date
2022-11-23
Country
United States
Brand
Viatris
Product
Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Viatris recalls

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    FDA · DrugViatris IncNationwide within the united statesOfficial notice →
  5. 2023-06-14
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    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.

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  7. 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,…

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    FDA · DrugViatris IncNationwide in the USAOfficial notice →
  9. 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 →
  11. 2022-05-18
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    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.

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All 12 Viatris recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-23
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    Adam's Polishes LLC recalls Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b)…

    CGMP Deviations: Other lots of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

    FDA · DrugAdam's Polishes LLCNationwide in the USAOfficial notice →
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    Adam's Polishes LLC recalls Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b)…

    Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL BASED HAND SANITIZER isopropyl alcohol 75% v/v to contain methanol.

    FDA · DrugAdam's Polishes LLCNationwide in the USAOfficial notice →
  4. US
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    Nephron Sterile Compounding Center LLC recalls PF-Neostigmine Methylsulfate Injection, USP 3 mg/3 mL (1 mg/mL) vial, Rx Only, Nephron 503B Outsourcing Facility 4500…

    CGMP Deviations: Potential for cross contamination due to product carry over.

    FDA · DrugNephron Sterile Compounding Center LLCNationwide in the USAOfficial notice →
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    ICU Medical Inc recalls 0.9% Sodium Chloride Injection, USP, 100 mL flexible container bag, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC…

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    Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.

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See all drugs & medical recalls →