Biomet, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2260-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 60 MM Item Number: 11-301301

Product Classification:

Class II

Date Initiated: June 2, 2021

Date Posted: August 18, 2021

Recall Number: Z-2260-2021

Event ID: 88304

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

Status: Terminated

Product Quantity: N/A

Code Information:

Lot Numbers/UDI : Lot Number UDI Number 626490 (01)00880304468030(17)310412(10)626490 679210 (01)00880304468030(17)310418(10)679210

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated