Medical device recalls Moderate risk

Stryker GmbH recalls Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463

Recall date
May 4, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2244-2018
FDA classification
Class II
Brand / firm
Stryker GmbH
Sold / distributed
AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD & TX

Why it was recalled

Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm

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

What was recalled

Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463

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