International safety notice
Urgent Field Safety Notice for LactoSorb RapidFlap by Biomet Orthopaedic LLC
Germany / BfArM · DEU · Mar 14, 2019
Key facts
| Title | Urgent Field Safety Notice for LactoSorb RapidFlap by Biomet Orthopaedic LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | LactoSorb RapidFlap |
| Manufacturer | Biomet Orthopaedic LLC |
| Models | 538610, 379800, CF04107, ZFA-2019-00009, 915-0020, 379910, 538880, 538180, 593410, 699490, 538480, 110900 and 66 more |
| Date | Mar 14, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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