Houston, TX, United States
Revive Rx LLC dba Revive Rx Pharmacy recalls
3 recalls recorded since 2018, most recently on 20 April 2024. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)2
Terminated or completed1
Class I (FDA)2
Ongoing Class I Drugs
- Recall started
- 20 April 2024
- Reason
- Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
- Distribution
- USA Nationwide
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0511-2024
- 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
Ongoing Class II Drugs
- Recall started
- 11 May 2023
- Reason
- Sub-potent Drug
- Distribution
- Nationwide in the US
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0771-2023
- 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.
Terminated Class I Drugs
- Recall started
- 11 February 2022
- Terminated
- 23 August 2024
- Reason
- Non-sterility; bacterial contamination identified as Paenibacillus lautus.
- Distribution
- Nationwide in the US.
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0648-2022
- HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only, Compounded By: Revive Rx 3831 Golf Dr., Houston, TX 77018, NDC: 88888-1739-01.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.