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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-2527-2026 - Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Catalog Number: 110040240 2 06/23/2026 FEI # 1000220733
Zimmer, Inc.
Z-2528-2026 - Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241 2 06/23/2026 FEI # 1000220733
Zimmer, Inc.
Z-2531-2026 - Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476 2 06/23/2026 FEI # 1000220733
Zimmer, Inc.
Z-2530-2026 - Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444 2 06/23/2026 FEI # 1000220733
Zimmer, Inc.
Z-2529-2026 - Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242 2 06/23/2026 FEI # 1000220733
Zimmer, Inc.
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