Lower riskMedical device recall · FDA · Published May 11, 2026
Zimmer Persona Revision Femoral Distal Augment Recall: Posterior Augment Found in Package
Zimmer recalls Persona Revision Femoral Distal Augment model 42-5572-066-10 due to posterior augment found in distal package. Affected patients should contact Zimmer for details.
“Zimmer Persona Revision Femoral Distal Augment Recall: Posterior Augment Found in Package.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49188-zimmer-persona-revision-femoral-distal-augment-recall-posterior-augment-found. Based on FDA recall #Z-2578-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2578-2026%22&limit=1).
Zimmer, Inc. voluntarily recalled Persona Revision Trabecular Metal Femoral Distal Augments on May 11, 2026, after a complaint revealed a posterior augment was found within the distal augment package, according to the FDA.
How to tell if you have it
Brand: Zimmer
Product Name: Persona Revision Trabecular Metal Femoral Distal Augment
Model/Catalog Number: 42-5572-066-10
UPC: 00889024561014
Lot Code: 66232947
The hazard
The firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package, according to the FDA.
Context
GovInfoNow's records show Zimmer, Inc. has 19 other recalls on record since August 25, 2022. Other recent recalls of similar products include U2 Total Knee System Femoral Offset Bushing Recall (March 19, 2026), Straumann Dental Implant Abutments Recall (March 27, 2026), and Howmedica OMNIFIT Series I Acetabular Insert Recall (July 30, 2026).
How to tell if you have this one
Check for the model number 42-5572-066-10 on the product label. The product was sold with lot number 66232947 and software version N/A.
Brand
Zimmer
Product
Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Contact Zimmer
Patients and medical staff should contact Zimmer directly for instructions on how to handle the recalled product.
How this recall unfolded
Recall timeline
FDA published this recall 51 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2578-2026 (May 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2578-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.