Zimmer Biomet G7 Acetabular System
Zimmer Biomet · Hip implants
No linked recall recordsLatest source check Oct 8, 2026
Loading MedWatcher information…
Loading MedWatcher information…
Devices and FDA recall records listed on MedWatcher for Zimmer Biomet.
This page covers the devices and recall records listed below, not the complete product catalogue or recall history. A recall may apply only to specific models, lots, or serial numbers.
Device and manufacturer names are linked using official product, UDI, or FDA records. The source links below show the supporting information.
Official records may use a legal name, brand, division, or shortened name. Similar names do not necessarily refer to the same manufacturer.
Zimmer Biomet · Hip implants
No linked recall recordsLatest source check Oct 8, 2026
Zimmer Biomet · Knee implants
No linked recall recordsLatest source check Oct 8, 2026
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
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, however, the implant inside the package is a Size G 46 mm, and vice versa.