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Zimmer Biomet, Inc. recalls fastener, fixation, nondegradable, soft tissue
Recalled March 21, 2018 · FDA recall Z-1009-2018 · Zimmer Biomet
Hazard
It was identified that the product was not assembled correctly causing the implant shaft to shift and fall out during the opening of the device, which potentially could break the device. · FDA Class II
Units
429 units
Sold at
TX, NC, FL, PA, IN, WI, VA, NY, NJ, AL, CT
Description
It was identified that the product was not assembled correctly causing the implant shaft to shift and fall out during the opening of the device, which potentially could break the device.
Product
fastener, fixation, nondegradable, soft tissue
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →