FDAFDA recall Z-2578-2026 · Jul 1, 2026
Zimmer, Inc.: Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Dis recall
Recall found
Product
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 for recall
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947
- 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.
- Recalling firm
- Zimmer, Inc., Warsaw, IN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-05-11
Source: openFDA enforcement record Z-2578-2026 · search recall number Z-2578-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.