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

DEWEI MEDICAL EQUIPMENT CO LTD 2022-12-14 Health critical FDA
Health · FDA · Recall #FDA-Z-0323-2023

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. 1 Stop using Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact DEWEI MEDICAL EQUIPMENT CO LTD 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
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.
Read the official FDA notice

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