HomeMedical Device recalls
Medium severity

Medline medical procedure kits, containing Medline Neuro Sponges (961 in total), NEURO,

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateMarch 19, 2026
ReportedMay 06, 2026
Recalling firmMedline Industries, LP
Country / regionUnited States IL

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.

Affected products

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