Official recall record
Dual Mobility Vivacit-E® Vitamin E Bearing
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-10-14
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Zimmer Biomet is conducting a medical device recall for one (1) lot of the Dual Mobility Vivacit-E® bearing due to a commingle. The outer package is labeled as a size G 46 mm, however, the implant inside the package is a size F 44 mm. One (1) complaint has been received that identified the size discrepancy at the point of use during the procedure. The defectiveness was discovered on September 19, 2025. Issue was identified through the complaints handling process.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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