Zimmer, Inc. recalls Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guid
See all recalls from Zimmer, Inc. →Recalled Product
Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444
Hazard / Issue
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: 110040444 ; UDI-DI (01)00889024681903(17)350531(10)097487 ; Lot Number 097487
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Off-Axis Alliance Glenoid, Left, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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