Plastic Surgery And Accessories Kit

Product
Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)
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.
Classification
Class I
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-03-19
Status
Open, Classified
Distribution
Worldwide distribution.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/87cc6604-d2b6-40bb-8739-7db351868777