Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: … Recall
Issued May 6, 2026 · Medline Industries, LP
In May 2026, Medline Industries, LP recalled the Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: …, 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
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
What you should do
- 1 Stop using Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: … 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.
Recall details
- Brand
- Medline Industries, LP
- Category
- Health
- Recall date
- May 6, 2026
- Units affected
- Not reported
- Sold at
- Worldwide distribution.
- Recall number
- FDA-Z-2037-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Medline Industries, LP has 50 recalls in our database, including 8 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.