Medical device recalls Moderate risk

Long Drill 1/4 inch Diameter 8 inch Length recalled over sterility concerns

Recall date
May 22, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Zimmer Biomet, Inc. recalls Long Drill 1/4 inch (6.4 mm) Diameter 8 inch (20.3 cm) Length, Item Number/EDI 00129100400, Nonsterile. orthopedic surg…
Recall number
Z-3146-2017
FDA classification
Class II
Brand / firm
Zimmer Biomet, Inc.
Sold / distributed
Nationwide in USA; Internationally to: Australia, Brazil, Canada, China, El Salvador, Germany, Guatemala, India, Japan, Panama, Malaysia, Mexico, Netherlands, South Korea, Singapore, Taiwan & Trinidad.

Why it was recalled

Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. The anomaly may be on or below the surface and can increase the risk of instrument fracture.

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

What was recalled

Long Drill 1/4 inch (6.4 mm) Diameter 8 inch (20.3 cm) Length, Item Number/EDI 00129100400, Nonsterile. orthopedic surgical instrument.

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