Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B Recall
Issued December 14, 2022 · DEWEI MEDICAL EQUIPMENT CO LTD
In December 2022, DEWEI MEDICAL EQUIPMENT CO LTD recalled the Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B, 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
Products were distributed in the United States without FDA authorization or clearance.
What you should do
- 1 Stop using Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact DEWEI MEDICAL EQUIPMENT CO LTD 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.
Recall details
- Brand
- DEWEI MEDICAL EQUIPMENT CO LTD
- Category
- Health
- Recall date
- December 14, 2022
- Units affected
- Not reported
- Sold at
- US Distribution in states to: CA, FL, KY, and MI.
- Recall number
- FDA-Z-0323-2023
- Made in
- China
- Issuing agency
- FDA
In context
- DEWEI MEDICAL EQUIPMENT CO LTD 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.