Medical device recalls Moderate risk

Zimmer GmbH recalls Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207

Recall date
April 8, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1427-2019
FDA classification
Class II
Brand / firm
Zimmer GmbH
Sold / distributed
The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.

Why it was recalled

An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

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

What was recalled

Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207

Get recall alerts

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

More recalls from: Zimmer GmbH