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Recall Observatory FDA recall evidence

Device product

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: EH BRONCHOSCOPY, Medline Kit Number/SKU DYNJT3270

Z-2010-2026

March 19, 2026

Class II

Product summary

Firm
Medline Industries, LP
Event
Event 98664
Status
Ongoing
Classification
Class II
Quantity
152 kits
Official record key
device-enforcement:Z-2010-2026

Official wording

Reason: 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.

Code information: UDI/DI each 10198459322235, UDI/DI case 40198459322236, Lot Numbers: 26AMF231, 25GMC304, 25DMF469.

Distribution pattern: Worldwide distribution.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out-of-specification