Revive Rx LLC dba Revive Rx Pharmacy: Drug Recall

Recall #D-0771-2023 · 05/11/2023

Class II: Risk

Recall Details

Recall Number: D-0771-2023
Classification: Class II
Product Type: Drug
Recalling Firm: Revive Rx LLC dba Revive Rx Pharmacy
Status: Ongoing
Date Initiated: 05/11/2023
Location: Houston, TX, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 45 Vials

Reason for Recall

Sub-potent Drug

Product Description

Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only, Compounded Drug Product By: Revive Rx, 3831 Golf Dr A, Houston, TX 77018, NDC: 99000-9278-64.

Distribution Pattern

Nationwide in the US

Other Recalls by Revive Rx LLC dba Revive Rx Pharmacy

Class I: Dangerous 04/20/2024

Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
Class I: Dangerous 02/11/2022

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

View all recalls by Revive Rx LLC dba Revive Rx Pharmacy →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.