FDAJune 7, 2017device

Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021), REF/Product Code RM*RS7F10PA, STERILE, Rx ONLY

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

The hazard

An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introducer Sheath was detected in a small quantity of the affected lot population, 0.01% (1 in 10, 000 units). This breach of the sterile barrier may compromise the sterility of the sheath.

What to do

FDA enforcement status: Terminated

Brands named

terumo medicalterumo

Recall history

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

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