ProgenaCare 2022-06-01 Health serious FDA
Health · FDA · Recall #FDA-Z-1137-2022
progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1)… Recall
Issued June 1, 2022 · ProgenaCare
In June 2022, ProgenaCare recalled the progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1)…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Inner pouch seal may be inadequate resulting in lack of sterility.
What you should do
- 1 Stop using progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1)… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact ProgenaCare to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- ProgenaCare
- Category
- Health
- Recall date
- June 1, 2022
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AL, GA, FL, TN, and TX. There was no foreign/military/government distribution.
- Recall number
- FDA-Z-1137-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- ProgenaCare has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.