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FDAFDA · Food and drugs·Recall number Z-2014-2026

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U

Published May 6, 2026 · Recall initiated: March 19, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the 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.

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Medline Industries, LP
Distributor
Worldwide distribution.
Lot
UDI/DI each 10193489634594, UDI/DI case 40193489634595, Lot Number: 24ILA931
Risk classification
Class II
Area (FDA)
device
Country
United States

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