FDAAugust 1, 2016device

Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture

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

The hazard

There is a potential for the needle to detach from the suture thread during surgery. If the needle becomes detached the defective suture will need to be replaced causing the wound to be sutured a second time.

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

Recall history

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

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