Recall
FDAHealthAugust 22, 2024

ProRx LLC — SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04

⚠️ Lack of Assurance of Sterility

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 22, 2024

Nationwide in the USA

What's affected?

Product
SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
Lot code
ProRx061424, BUD 12/13/2024

Additional details

ProRx061424, BUD 12/13/2024

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 1,960 vials.

View original FDA notice →

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