FDA Enforcement Class II Ongoing

TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E

Recall: Z-1630-2024 · Reported May 1, 2024

Enforcement

Recall Number
Z-1630-2024
Event ID
94215
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Howmedica Osteonics Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 1, 2024
Initiation Date
February 27, 2024
Classification Date
April 25, 2024
Address
325 Corporate Dr, N/A, Mahwah, NJ, 07430-2006, United States

Description

TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E

Reason

The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell

Code Info

UDI-DI: (01)07613327381023(17)290313(10) Lot Number: 14876553 14876552

Distribution

Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UK

Quantity

3 units