Quick Facts at a Glance
- Recall Date
- May 11, 2026
- Hazard Level
- HIGH
- Brand
- Zimmer
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. 42-5572-066-10, UDI-DI (01)00889024561014(17)331103(10)66232947, Lot number 66232947
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 11, 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
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
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: Letter
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Full Description
Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes Component: N/A. Reason: Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.. Classification: Class II. Quantity: 12. Distribution: Refer to the attached ZFA 2026-00088_Initial Consignee List and ZFA 2026-00088_Initial Distribution History containing the distribution and the identification of the affected consignees.
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Safety Guide
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