medical MODERATE Updated 2026-07-01

Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System, Large, Augment, Off-

See all recalls from Zimmer, Inc. →

Recalled Product

Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242

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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: Model No. 110040242 ; UDI-DI (01)00889024681989(17)350601(10)099471 ; Lot Number 099471 Model No. 110040242 ; UDI-DI (01)00889024681989(17)350614(10)099473 ; Lot Number 099473 Model No. 110040242 ; UDI-DI (01)00889024681989(17)350804(10)099474 ; Lot Number 099474 Model No. 110040242 ; UDI-DI (01)00889024681989(17)350806(10)099475 ; Lot Number 099475

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for Off-Axis Comprehensive Shoulder System, →

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View official government recall

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Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System Small, Augment, Off-A

2026-07-01 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.