Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM, Reorder Number… Recall
Issued February 22, 2023 · MEDLINE INDUSTRIES, LP - Northfield
In February 2023, MEDLINE INDUSTRIES, LP - Northfield recalled the Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM, Reorder Number…, a serious 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
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
What you should do
- 1 Stop using Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM, Reorder Number… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MEDLINE INDUSTRIES, LP - Northfield 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
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- February 22, 2023
- Units affected
- Not reported
- Sold at
- Nationwide
- Recall number
- FDA-Z-1125-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- MEDLINE INDUSTRIES, LP - Northfield has 108 recalls in our database, including 12 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.