FDAClass IJuly 9, 2025

Buffered Penicillin G Potassium for Injection recall: Labeling Error

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by…

Why was Buffered Penicillin G Potassium for Injection recalled?

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 should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot # PG4360, PG4362, Exp. 11/30/2027

Product
Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by…
Recalling firm
Sandoz Inc
Quantity
unknown
Distribution
Nationwide in the USA
Recall date
July 9, 2025
Classification
Class I
Status
Ongoing
Agency
FDA (drug)
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