Recall
FDAHealthOctober 15, 2025

ProRx LLC — Semaglutide Injection, 6mg/2.4mL (2.5 mg/mL), 2.4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-08

⚠️ Lack of Assurance of Sterility

Is this relevant to me?

Geography
TX, UT
Source agency
FDA
Category
Health
Published
October 15, 2025

TX and UT

What's affected?

Product
Semaglutide Injection, 6mg/2.4mL (2.5 mg/mL), 2.4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-08
Lot code
Prorx051425-2

Additional details

Lot Prorx051425-2, Lot Prorx051425-3 and Lot Prorx051425-4

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 8,310 vials.

View original FDA notice →

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