International safety notice
Lot recall of various sterile-packaged knee and hip implants, Zimmer Biomet
Germany / BfArM · DEU · May 10, 2016
Key facts
| Title | Lot recall of various sterile-packaged knee and hip implants, Zimmer Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of various sterile-packaged knee and hip implants, Zimmer Biomet |
| Manufacturer | Lot recall of various sterile-packaged knee and hip implants, Zimmer Biomet |
| Models | 62100778, 61792646, 00726006428, 61914847, 61770810, 62119907, 62051904, 61747148, 61762597, 61759779, 61809003, 61868679 and 1211 more |
| Date | May 10, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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