G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty
FDA Recall Z-0007-2023 · Posted 2022-10-05
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Recalling FirmZimmer, Inc.
Recall StatusOpen, Classified
Product CodeOQI
Date Initiated2022-08-25
Product Quantity56 US
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.
Firm Action
On August 25, 2022, the firm notified affected customers via Urgent Medical Device Recall letters.
Customers were instructed to quarantine all affected product. Zimmer Biomet sales representatives will remove the affected product from customer facilities.
Customers should ensure that affected personnel are aware of the recall, and also notify any recipients if the product has been further distributed.
If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
Domestic distribution US nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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