FDA Recall Open, Classified

Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.

Recall: Z-0549-2025 · Initiated October 30, 2024

Recall

Recall Number
Z-0549-2025
Event Number
95653
Firm
INCIPIO DEVICES avenue des Paquiers 16 St-Blaise Switzerland
FEI Number
3013223655
Product Code
HWA
Status
Open, Classified
Root Cause
Process change control
Initiated
October 30, 2024
Posted
November 25, 2024

Description

Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.

Reason

Recalled lot does not meet specification and has reported incidents of fracture of the TIG weld.

Action

Consignees were mailed a recall notification titled URGENT ADVISORY NOTICE dated 10/30/2024. The notification instructs consignees to examine their inventory and identify all affected devices for quarantine immediately. Consignees are to complete and return the Recall Response Form to Incipio Devices at [email protected] to facilitate the return of recalled devices and issuance of a FedEx return label. Returned devices should be sent back in their original packaging if unused and properly decontaminated and sterilized if being sent back used. Consignees with any questions should contact Incipio Devices by phone at +41 32 754 34 34 or by email at [email protected].

Distribution

US Nationwide distribution in the state of TN.

Quantity

100 units