Medline Industries, LP 2026-06-24 Health serious FDA
Health · FDA · Recall #FDA-Z-2496-2026
MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN, Medline Kit Number/SKU… Recall
Issued June 24, 2026 · Medline Industries, LP
In June 2026, Medline Industries, LP recalled the MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN, Medline Kit Number/SKU…, 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 Dana Whitfield, RecallCheckr
What this means for you
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
What you should do
- 1 Stop using MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN, Medline Kit Number/SKU… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medline Industries, LP 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
- Category
- Health
- Recall date
- June 24, 2026
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of AE, BB, BM, BS, CA, CY, GU, NL, PA, QA, SA, VI.
- Recall number
- FDA-Z-2496-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Medline Industries, LP has 62 recalls in our database, including 8 rated Critical.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.