FDA recall, , Moderate risk
Persona Revision Trabecular Metal Femoral Distal Augment
The Persona Revision Trabecular Metal Femoral Distal Augment may contain a posterior augment inside its package.
Summary by Recall Canary from the FDA notice
What happened
Zimmer, Inc. of Warsaw, Indiana, recalled the Persona Revision Trabecular Metal Femoral Distal Augment, model 42-5572-066-10, after receiving a complaint with no clinical impact in which a posterior augment was found within the distal augment package. The recall began May 11, 2026, and was added to the FDA's Enforcement Report on June 24, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and lot code listed under your product.
Persona Revision Trabecular Metal Femoral Distal Augment
- Model number
- 42-5572-066-10
- Lot code
- 66232947
Recall details
- Company began the recall
- Sold in
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.
- Company
- Zimmer, Inc.Warsaw, Indiana
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99073
- Recall number
- Z-2578-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
