Quick Facts at a Glance
- Recall Date
- May 20, 2026
- Hazard Level
- HIGH
- Brand
- Zimmer
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Zimmer
- Model numbers
- Lot Code: Model No. 110040240, UDI-DI (01)00889024681965(17)350601(10)099457, Lot Number 099457 Model No. 110040240, UDI-DI (01)00889024681965(17)350712(10)099458, Lot Number 099458
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 20, 2026
Reported by FDA DEVICE
July 1, 2026
RecallRadar source check
July 7, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Zimmer, Inc. or your healthcare provider for instructions. Notification method: N/A
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Full Description
Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Catalog Number: 110040240. Reason: Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.. Classification: Class II. Quantity: 474 units. Distribution: US Nationwide distribution.
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Safety Guide
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Read: How to Get Refunds and ReplacementsWant to Know First?
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