International safety notice
Biomet
United Kingdom / MHRA · GBR · Mar 12, 2019
Key facts
| Title | Biomet |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | LactoSorb RapidFlap |
| Manufacturer | Biomet |
| Models | 538250, 538680, 379800, 662380, 615380, 379870, 699540, 379810, 538920, 110910, 662300, 538370 and 66 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Mar 12, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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