Recall
FDAHealthMarch 19, 2026

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

⚠️ 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.

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
March 19, 2026

Worldwide distribution.

What's affected?

Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINE PACK-LF, Medline Kit Number/SKU PHS719414B
Lot code
22GBF198

Additional details

UDI/DI each 10889942214112, UDI/DI case 40889942214113, Lot Numbers: 22GBF198, 22DBU132, 22ABJ303, 21GBV167, 21GBV186, 21BBL371.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 104 kits.

View original FDA notice →

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