Medical Device

Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)

Recall date: 2026-05-06 · Source: FDA_DEVICE

Brand / Firm

Product

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.

Units affected

22116 kits

Description

Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)

View official recall notice →