Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026
Brand Name: Persona Revision Product Name: Persona Revision� Trabecular Metal� Femoral Distal Augment Model/Catalog…
Zimmer, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zimmer, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- Brand NamePersona
- Revision Product NamePersona Revision� Trabecular Metal� Femoral
- Distal Augment Model/Catalog Number42-5572-066-10
- Software VersionN/A
- Product DescriptionPersona Revision� Trabecular Metal� Femoral Distal Augment Size 9, 9+ 10mm
- Thicknes ComponentN/A
- Lot codes and dates
- Lot CodeModel No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947
- Amount recalled
- 12
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Why it was recalled
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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