International safety notice
Guidant recalls Omnilink Peripheral Stent Systems
Germany / BfArM · DEU · Aug 12, 2005
Key facts
| Title | Guidant recalls Omnilink Peripheral Stent Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Guidant recalls Omnilink Peripheral Stent Systems |
| Manufacturer | Guidant recalls Omnilink Peripheral Stent Systems |
| Models | 12-AIJG-ZE.5, 92221222, 32221222, 12-AJG-ZØS, 12-AIJß-ZES, 12-AUG-20ØS |
| Date | Aug 12, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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