Zimmer, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0007-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty

Product Classification:

Class II

Date Initiated: August 25, 2022

Date Posted: October 12, 2022

Recall Number: Z-0007-2023

Event ID: 90858

Reason for Recall:

The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include non-clinically or clinically significant extension of surgery, or infection leading to surgical intervention.

Status: Ongoing

Product Quantity: 56 US

Code Information:

Item No. 010000663 UDI-DI: 00880304524224 Lots: 7286477 7289929 7296576 7296633 7301697 Exp. 21-Jul-32 Item No. 010000667 UDI-DI: 00880304524262 Lot: 7253325 Exp. 13-Jun-32

Distribution Pattern:

Domestic distribution US nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated