Revive Rx LLC dba Revive Rx Pharmacy: Drug Recall
Recall #D-0648-2022 · 02/11/2022
Class I: Dangerous
Recall Details
- Recall Number
- D-0648-2022
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Revive Rx LLC dba Revive Rx Pharmacy
- Status
- Terminated
- Date Initiated
- 02/11/2022
- Location
- Houston, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 115 vials
Reason for Recall
Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Product Description
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.
Distribution Pattern
Nationwide in the US.
Other Recalls by Revive Rx LLC dba Revive Rx Pharmacy
- Class I: Dangerous 04/20/2024
- Class II: Risk 05/11/2023
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.