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Class I

  • The FDA’s most serious category — a reasonable probability of serious harm or death.
  • Refunds don't require a receipt, and you don't need proof of purchase.
  • FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14
Check with your pharmacist Filed 2025-07-09

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

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781-6136-94.

Check these codes: Lot # PG4360, PG4362, Exp. 11/30/2027

unknown · distributed nationwide in the usa Recall D-0570-2025 on FDA.gov ↗
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