Revive Rx LLC dba Revive Rx Pharmacy: Drug Recall
Recall #D-0511-2024 · 04/20/2024
Class I: Dangerous
Recall Details
- Recall Number
- D-0511-2024
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Revive Rx LLC dba Revive Rx Pharmacy
- Status
- Ongoing
- Date Initiated
- 04/20/2024
- Location
- Houston, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 751 vials
Reason for Recall
Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
Product Description
Tirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded Product By: Revive RX Pharmacy, 3831 Golf Dr A, Houston, TX 77018, internally assigned NDC 99000-9278-64
Distribution Pattern
USA Nationwide
Other Recalls by Revive Rx LLC dba Revive Rx Pharmacy
- Class II: Risk 05/11/2023
- Class I: Dangerous 02/11/2022
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.