International safety notice
Lot recall of various polyethylene implants, Zimmer Biomet
Germany / BfArM · DEU · Mar 3, 2017
Key facts
| Title | Lot recall of various polyethylene implants, Zimmer Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of various polyethylene implants, Zimmer Biomet |
| Manufacturer | Lot recall of various polyethylene implants, Zimmer Biomet |
| Models | 708440, 183400, 183522, 456240, 534820, 242470, 699920, 459000, 455600, 458030, 376180, 542210 and 2063 more |
| Date | Mar 3, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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