Recall
FDAHealthAugust 22, 2024

ProRx LLC — SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01

⚠️ 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 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01
Lot code
ProRx052424

Additional details

Lot #: ProRx052424, BUD 11/23/2024 ProRx060724, BUD 12/06/2024 ProRx061124, BUD 12/10/2024 ProRx061924, BUD 12/18/2024

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 8,396 vials.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.