Product Safety Recalls

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Biomet, Inc. Recall 91866

Description: G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462

Biomet, Inc. Recall 91866 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1284-2023
Event ID91866
Event DescriptionG7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Product TypeDevices
DistributionUS Distribution to states of: AZ, FL, GA, MI, NE, and TX.
Quantity12 units
Recall ReasonThe outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Device Classification20230329
Device Code InfoUDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960
Center Classification Date20230323
Recall Initiation Date20230206
Recalling FirmBiomet, Inc.
Initial Notification Letter
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