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Medium risk Drugs & MedicationsClass II

Zimmer, Inc. Recall

Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241

Updated May 20, 2026

Zimmer, Inc. is recalling Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241. Hazard: Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Is the Zimmer, Inc. recalled? Yes. This product was recalled by FDA on May 20, 2026. Details below.

What is recalled

Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

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

Brands affected

Zimmer, Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-2528-2026
Classification
Class II
Recalled
May 20, 2026
Read the official notice

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