PlainRecalls
FDA Devices Moderate Class II Terminated

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size C, 70 MM Item Number: 11-301333

Reported: August 18, 2021 Initiated: June 2, 2021 #Z-2271-2021

Product Description

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size C, 70 MM Item Number: 11-301333

Reason for Recall

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

Details

Recalling Firm
Biomet, Inc.
Units Affected
12 units
Distribution
US Nationwide distribution.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Arcos Modular Revision Hip System High Offset Cone Prox Body, Size C, 70 MM Item Number: 11-301333. Recalled by Biomet, Inc.. Units affected: 12 units.
Why was this product recalled?
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention
Which agency issued this recall?
This recall was issued by the FDA Devices on August 18, 2021. Severity: Moderate. Recall number: Z-2271-2021.