Pro-Dex Inc 2023-04-26 Health serious FDA
Health · FDA · Recall #FDA-Z-1391-2023
KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly… Recall
Issued April 26, 2023 · Pro-Dex Inc
In April 2023, Pro-Dex Inc recalled the KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Incorrect Unique Device Identifier/GTIN code was used on product.
What you should do
- 1 Stop using KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Pro-Dex Inc 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
- Pro-Dex Inc
- Category
- Health
- Recall date
- April 26, 2023
- Units affected
- Not reported
- Sold at
- U.S. Nationwide distribution in the state of FL.
- Recall number
- FDA-Z-1391-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Pro-Dex Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.