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Persona Revision Femoral Distal Augment
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MEDICAL DEVICE RECALLMODERATE

Persona Revision Femoral Distal Augment

Zimmer is recalling the Persona Revision Femoral Distal Augment (model 42-5572-066-10) due to a packaging error.

What to do

Check the contents of your product packaging to ensure the correct component is present. If you identify a posterior augment in your distal augment package, contact your Zimmer representative or the company for a replacement.

Posted
Updated
Recall No.
Z-2578-2026
Agency
Firm
Zimmer, Inc.
Recall ID
99073
Status
ONGOING

Why it was recalled

Zimmer is recalling the Persona Revision Trabecular Metal Femoral Distal Augment due to a packaging error where a posterior augment was incorrectly included in the distal augment package. The affected product is model 42-5572-066-10.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

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

UPC
00889024561014, 66232947, 66232947
Recall #
Z-2578-2026

Other recent recalls from Zimmer, Inc.

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Editorial summary by Recall Canary · last updated 2026-06-25 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification