FDA recall record

Revive Rx LLC dba Revive Rx Pharmacy HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj. recall — FDA D-0648-2022

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

Class Iclassification
D-0648-2022official record ID
Feb 23, 2022report date

Recall record at a glance

Official recordD-0648-2022
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmRevive Rx LLC dba Revive Rx Pharmacy
Report dateFeb 23, 2022
Recall initiation dateFeb 11, 2022
Quantity115 vials
LocationHouston, TX, United States

Official 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.

Why the product was recalled

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

Distribution information

Nationwide in the US.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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