International safety notice
Recall of the NEWAY DR pacemakers from Sorin
Germany / BfArM · DEU · Jul 17, 2007
Key facts
| Title | Recall of the NEWAY DR pacemakers from Sorin |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the NEWAY DR pacemakers from Sorin |
| Manufacturer | Recall of the NEWAY DR pacemakers from Sorin |
| Models | 26C00121, 26D00163, 2000175, 26D00168, 26C00104, 00554890772, 1623520, 26D00179, 26C00105, 2000202, 26C00125, 26D00132 and 20 more |
| Date | Jul 17, 2007 |
| 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