FDAOctober 31, 2018device

Protexis Neoprene Surgical Glove, Size 6.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

What to do

FDA enforcement status: Terminated

Brands named

cardinal health 200cardinalcardinal health

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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