Dual Mobility Vivacit-E® Vitamin E Bearing
Brand(s)
Last updated
Summary
Product
Dual Mobility Vivacit-E® Vitamin E Bearing
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Dual Mobility Vivacit-E® Vitamin E Bearing | 67160480 | 110031013 |
Issue
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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Orthopaedics
Companies
Zimmer Inc.
1800 West Center Street, Warsaw, Indiana, United States, 46580
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-78295
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