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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

Revive Rx LLC dba Revive Rx Pharmacy 2022-02-23 Health critical FDA
Health · FDA · Recall #FDA-D-0648-2022

HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV… Recall

Issued February 23, 2022 · Revive Rx LLC dba Revive Rx Pharmacy

In February 2022, Revive Rx LLC dba Revive Rx Pharmacy recalled the HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

What you should do

  1. 1 Stop using HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Revive Rx LLC dba Revive Rx Pharmacy to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Revive Rx LLC dba Revive Rx Pharmacy
Category
Health
Recall date
February 23, 2022
Units affected
Not reported
Sold at
Nationwide in the US.
Recall number
FDA-D-0648-2022
Made in
United States
Issuing agency
FDA

In context

  • Revive Rx LLC dba Revive Rx Pharmacy has 1 recall in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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