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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

Sandoz Inc 2025-07-09 Health critical FDA
Health · FDA · Recall #FDA-D-0570-2025

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units),… Recall

Issued July 9, 2025 · Sandoz Inc

In July 2025, Sandoz Inc recalled the Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units),…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit

What you should do

  1. 1 Stop using Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units),… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Sandoz Inc 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
Sandoz Inc
Category
Health
Recall date
July 9, 2025
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0570-2025
Made in
United States
Issuing agency
FDA

In context

  • Sandoz Inc has 3 recalls in our database, including 2 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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