Home / Recalls / Medical Devices
Zimmer GmbH recalls Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630
Recalled May 29, 2019 · FDA recall Z-1481-2019 · Zimmer
Hazard
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. · FDA Class II
Units
N/A
Sold at
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.
Description
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Product
Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630
Manufacturer(s)
Zimmer GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →