PlainRecalls
FDA Drug Critical Class I Terminated

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.

Reported: February 23, 2022 Initiated: February 11, 2022 #D-0648-2022

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.

Reason for Recall

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

Details

Units Affected
115 vials
Distribution
Nationwide in the US.
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
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.. Recalled by Revive Rx LLC dba Revive Rx Pharmacy. Units affected: 115 vials.
Why was this product recalled?
Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 23, 2022. Severity: Critical. Recall number: D-0648-2022.