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Zimmer, Inc. recalls Identity Shoulder System Resection Planer 35mm Resection Planer
Recalled February 15, 2023 · FDA recall Z-1098-2023 · Zimmer
Hazard
Two planers were found to be unusable during sawbones shoulder training. · FDA Class II
Units
84 units
Sold at
US Nationwide distribution in the states of AR, CA, IL, MI, NJ, NY, OK, PA, TX, and WA.
Description
Two planers were found to be unusable during sawbones shoulder training.
Product
Identity Shoulder System Resection Planer 35mm Resection Planer
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →