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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.

Recalled
Listed
Updated
Recall No.
Z-2578-2026
Agency
FDA
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.

Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment

Lot code
42-5572-066-10, 66232947
UDI-DI
00889024561014, 66232947, 66232947
Model/Catalog number
42-5572-066-10

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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