MEDLINE INDUSTRIES, LP - Northfield 2024-12-04 Health serious FDA
Health · FDA · Recall #FDA-Z-0513-2025
MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; … Recall
Issued December 4, 2024 · MEDLINE INDUSTRIES, LP - Northfield
In December 2024, MEDLINE INDUSTRIES, LP - Northfield recalled the MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; …, 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 connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
What you should do
- 1 Stop using MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; … 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.
Official remedy (Voluntary):
Recall details
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- December 4, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
- Recall number
- FDA-Z-0513-2025
- 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 737th Health recall we've logged in 2024.