FDA-Device2023-02-15Class II
Identity Shoulder System Resection Planer 35mm Resection Planer
Hazard
Two planers were found to be unusable during sawbones shoulder training.
Sold states
US Nationwide distribution in the states of AR, CA, IL, MI, NJ, NY, OK, PA, TX, and WA.
Affected count
84 units
Manufactured in
1800 W Center St, Warsaw, IN, United States
Products
Identity Shoulder System Resection Planer 35mm Resection Planer
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1098-2023More Zimmer, Inc. recalls
- FDA-Device2026-07-01Zimmer Off-Axis Comprehensive Shoulder System reamer guide recalled for breakage risk
- FDA-Device2026-07-01Zimmer Off-Axis Alliance Glenoid Reamer Guide recalled for plastic breakage risk during surgery
- FDA-Device2026-07-01Zimmer Persona Revision Femoral Distal Augment recalled for wrong component in package
- FDA-Device2026-07-01Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444
- FDA-Device2026-07-01Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242
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