Class II

Medical Device Recall: Medline medical procedure kits, containing Medline Neuro Sponges (961 in total), NEURO,

Medline Industries, LP · March 19, 2026

Reason for Recall

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.

Distribution

Worldwide distribution.

Quantity Affected

538201 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2033-2026

Status: ongoing

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