RecalledThisWeek Search
Medium risk Medical DevicesClass II

Medline Neuro Sponges Kit Recall

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U

Updated March 19, 2026

Medline is recalling certain medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels, which may not meet safety specifications. Endotoxin contamination can trigger serious inflammatory reactions in patients.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on March 19, 2026. Details below.

What is recalled

Medline medical procedure kits labeled ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U, containing Medline Neuro Sponges.

Am I affected

You're affected if you have an ANGIO PACK-LF kit with Medline Kit Number/SKU DYNJ0774765U. Check the label on your medical procedure kit.

What to do right now

Stop using this product immediately. Contact Medline Industries, LP to report that you have the recalled kit and for instructions on return or replacement.

The hazard

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.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2014-2026
Classification
Class II
Recalled
March 19, 2026
Read the official notice

Get free recall alerts

New Medical Devices recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Medical Devices recalls