FDA Enforcement Class II Terminated

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size D, 80 MM Item Number: 11-301354

Recall: Z-2275-2021 · Reported August 18, 2021

Enforcement

Recall Number
Z-2275-2021
Event ID
88304
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Biomet, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 18, 2021
Initiation Date
June 2, 2021
Classification Date
August 12, 2021
Termination Date
July 6, 2022
Address
56 E Bell Dr, N/A, Warsaw, IN, 46582-6989, United States

Description

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size D, 80 MM Item Number: 11-301354

Reason

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code Info

Lot Numbers/UDI : 880960 (01)00880304474307(17)310504(10)880960

Distribution

US Nationwide distribution.

Quantity

12 units