International safety notice
Recall for Hemovac Autotransfusion System, Zimmer
Germany / BfArM · DEU · Mar 27, 2008
Key facts
| Title | Recall for Hemovac Autotransfusion System, Zimmer |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Hemovac Autotransfusion System, Zimmer |
| Manufacturer | Recall for Hemovac Autotransfusion System, Zimmer |
| Models | ΟΗ55505005, 60143328, 602380, 60088746, 00265505005, 60171635, 602557Ώ, 00255505006, 33435900, 60278484, 00255506005, 60255721 and 276 more |
| Date | Mar 27, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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