RecalledThisWeek Search
High risk Medical DevicesClass II

Medline Spine Pack Neuro Sponges Recall

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINE PACK-LF, Medline Kit Number/SKU PHS719414B

Updated March 19, 2026

Medline is recalling medical procedure kits containing Neuro Sponges (SPINE PACK-LF, SKU PHS719414B) because they may have higher-than-expected endotoxin levels. Endotoxin contamination can cause serious inflammation or infection during surgical procedures.

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 SPINE PACK-LF, Medline Kit Number/SKU PHS719414B, containing Medline Neuro Sponges.

Am I affected

You're affected if you have a Medline procedure kit labeled SPINE PACK-LF with SKU PHS719414B that contains Medline Neuro Sponges.

What to do right now

Stop using this product immediately. Contact Medline Industries, LP, or your supplier for instructions on returning the affected kit.

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-2012-2026
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