Medical device recalls Moderate risk

Zimmer Biomet, Inc. recalls Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone…

Recall date
August 3, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-3252-2018
FDA classification
Class II
Brand / firm
Zimmer Biomet, Inc.
Sold / distributed
AZ CO FL FL GA LA MA MA MO NY SC TX

Why it was recalled

Expiration date incorrectly listed on the label

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for use in: Shoulder, Foot and Ankle, Knee, Hand and Wrist and Hip repair.Stainless Steel, Sterile Item Number: 110016992

Get recall alerts

Free email alert whenever Zimmer Biomet, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Zimmer Biomet, Inc.