FDAJuly 27, 2017device

A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, Inc. Dover, OH 44622 Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.

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

The hazard

Updated on-device label and 3 pages of an updated Operator/Service Manual. Also, decrease from 3.8 meters (m) to 1.0 separation distance between the device and RF communication equipment.

What to do

FDA enforcement status: Terminated

Brands named

zimmer surgicalzimmer

UPCs

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Recall history

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

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