United StatesThe affected product is Zimmer Persona Revision Trabecular Metal Femoral Distal Augment (Model/Catalog No. 42-5572-066-10; size 9, 9+ 10 mm thickness; Lot number 66232947; UDI-DI (01)00889024561014(17)331103(10)66232947). It was recalled because a complaint reported a posterior augment was found inside the distal augment package; the recall is ongoing and 12 units were distributed to the listed consignees.
What's being recalled
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
Recalling firm: Zimmer, Inc., Warsaw, IN, United States.
How to identify it
Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947
The hazard
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
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.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)