International safety notice
Biomet (Zimmer)
United Kingdom / MHRA · GBR · Jun 27, 2019
Key facts
| Title | Biomet (Zimmer) |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Ultra-Drive® Hose/Drape Assembly and Ultra-Drive® Irrigation Tubing Assembly |
| Manufacturer | Biomet (Zimmer) |
| Models | 211638, 211172, 210002, 210488, ZFA2018-00634, 216610, 210972, 214994, 211325, 214499, 221437, 214051 and 51 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Jun 27, 2019 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1