Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm
FDA Recall Z-1131-2026 · Posted 2026-01-20
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Recalling FirmTyber Medical
Recall StatusOpen, Classified
Product CodeHRS
Date Initiated2025-12-19
Product Quantity100 units
Reason for Recall
The supplier manufactured anatomical left plates with an incorrect thread orientation.
Firm Action
On December 19, 2025, an URGENT MEDICAL DEVICE REMOVAL NOTIFICATION email was sent to their only customer. Actions to be taken:
1. Acknowledge the receipt of this communication via email correspondence to
[email protected]
2. Further distribute this communication through notifying the accounts that have received the
identified devices.
3. Identify via product label and quarantine the impacted devices under DePuy Synthes control all
devices that have not been distributed for sale. An RMA will be provided for the return of goods
to Tyber Medical.
4. Identify via product label and quarantine the impacted devices that have been distributed. An
RMA will be provided for the return of goods to Tyber Medical.
5. Complete the customer response form following this notification, or provide written
notification, and return it to Tyber Medical via email correspondence to [email protected]. A sub-notification letter was also provided to the distributor to provide to customers with the following actions:
1. Identify via product label and quarantine the impacted devices in your possession.
2. Complete the subsequent Acknowledgement and Receipt From and return it to DePuy Synthes
via email correspondence, with Tyber Medical copied at [email protected]
3. Return the impacted product to DePuy Synthes for replacement.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the state of PA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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