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FDAAugust 21, 2019device

2.0MM BALL NOSE GUIDE WIRE, Item Nos. 281017006 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.

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

The hazard

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00887868029448

Recall history

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

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2.0MM BALL NOSE GUIDE WIRE, Item Nos. 281017006 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices. — Recall Details · AllClear