Recall
FDAHealthAugust 22, 2024

ProRx LLC — Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01

⚠️ 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
Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01
Lot code
ProRx040924-1

Additional details

Lot # ProRx040924-1, BUD 10/08/2024

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 37 vials.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.