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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Amneal Pharmaceuticals of New York, LLC 2023-05-31 Health moderate FDA
Health · FDA · Recall #FDA-D-0756-2023

Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular,… Recall

Issued May 31, 2023 · Amneal Pharmaceuticals of New York, LLC

In May 2023, Amneal Pharmaceuticals of New York, LLC recalled the Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular,…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Labeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary packaging only). Incorrect NDC Number 70121-1573-1; Correct NDC Number 70121-1574-1.

What you should do

  1. 1 Stop using Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Amneal Pharmaceuticals of New York, LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Amneal Pharmaceuticals of New York, LLC
Category
Health
Recall date
May 31, 2023
Units affected
Not reported
Sold at
Nationwide in the USA and PR
Recall number
FDA-D-0756-2023
Made in
United States
Issuing agency
FDA

In context

Read the official FDA notice

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