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G7 Acetabular Liner

Biomet Orthopedics, LLC · Model 010000721 · UDI-DI 00880304524804

LPH JDI OQG OQH OQI PBI LZO LWZ KWZ Prescription

510(k) clearances

89,776

Adverse events (195 deaths)

297

Recalls

265

Facilities

Recalls

Date	Firm	Reason
2026-01-05	Encore Medical, LP	942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discr
2025-09-26	Zimmer, Inc.	Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, howe
2025-09-26	Zimmer, Inc.	Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, howe
2025-09-09	BioPro, Inc.	Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is impla
2025-09-09	BioPro, Inc.	Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is impla
2025-06-12	Encore Medical, LP	Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
2025-06-12	Encore Medical, LP	Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
2025-03-25	Conformis Inc.	The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
2024-12-31	Exactech, Inc.	Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
2024-09-19	Novosource, LLC	Mislabeled: Packaged in a box labeled as 32 long but containing a 28 long head by physical marking, may result in joint instability if implanted

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.