Class II recallOngoing

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

FDA · FDA event 99073 · Posted Jun 24, 2026

Published Jun 24, 2026Updated Oct 8, 2026Source last checked: 2026-10-08 16:03:16 UTC

What happened

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

Who may be affected

People using a product, model, software version, lot, or UDI listed in the affected-products table and official FDA record.
A mention of the device family does not mean every unit is affected. Compare the identifiers on your product with the official source.

What the official notice recommends

On May 11, 2026, the firm began notifying consignees via letters titled "URGENT MEDICAL DEVICE RECALL."
Customers were instructed to review the notification and ensure affected personnel are aware of the contents.
If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine affected product. The sales representative will remove the affected product from your facility.
If product has been further distributed, provide your customers with the recall notice and ensure documentation.

The official notice takes precedence over this summary. Talk to your clinician before changing prescribed therapy.

Affected products and models

This FDA record lists Persona Revision Trabecular Metal Femoral Distal Augment by Zimmer Biomet.

Products affected by FDA event 99073
Model	Description	Lot / serial range	Manufactured	Status
Z-2578-2026 · 42-5572-066-10 · N/A	Persona Revision Trabecular Metal Femoral Distal Augment	Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947	Not provided in the normalized record	Ongoing

Distribution: 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.
Units affected: See official FDA record
Category: Knee implants

Timeline

May 11, 2026
Recall initiated
Date recorded by the FDA.
Jun 24, 2026
Posted by FDA
The recall event appeared in the FDA source.
Oct 8, 2026
Last checked
MedWatcher last reconciled this record with the openFDA export.

Primary source

U.S. Food and Drug Administration

Identifier: 99073
Published: Jun 24, 2026
Source checked: 2026-10-08 16:03:16 UTC

Official openFDA device-recall record. The FDA source takes precedence over this normalized summary.

View official record

How MedWatcher checks these sources

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Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

FDA · FDA event 99073 · Posted Jun 24, 2026

Published Jun 24, 2026Updated Oct 8, 2026Source last checked: 2026-10-08 16:03:16 UTC

Affected products and models

This FDA record lists Persona Revision Trabecular Metal Femoral Distal Augment by Zimmer Biomet.

Products affected by FDA event 99073
Model	Description	Lot / serial range	Manufactured	Status
Z-2578-2026 · 42-5572-066-10 · N/A	Persona Revision Trabecular Metal Femoral Distal Augment	Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947	Not provided in the normalized record	Ongoing

Distribution

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.

Units affected

See official FDA record

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FDA · FDA event 98342Posted Mar 10, 2026

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

Follow Persona Revision Trabecular Metal Femoral Distal Augment

What happened

Who may be affected

What the official notice recommends

Affected products and models

Timeline

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

Follow Persona Revision Trabecular Metal Femoral Distal Augment

What happened

Who may be affected

What the official notice recommends

Affected products and models

Timeline

What happened

Who may be affected

What to do

What the official notice recommends

Affected products and models

Timeline

What happened

Who may be affected

What to do

What the official notice recommends

Affected products and models

Timeline