International safety notice
Lot Recall for the Cruiser Hydro Coronary and Peripheral Artery Guide Wire, Biotronik
Germany / BfArM · DEU · Nov 18, 2011
Key facts
| Title | Lot Recall for the Cruiser Hydro Coronary and Peripheral Artery Guide Wire, Biotronik |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Cruiser Hydro Coronary and Peripheral Artery Guide Wire, Biotronik |
| Manufacturer | Lot Recall for the Cruiser Hydro Coronary and Peripheral Artery Guide Wire, Biotronik |
| Models | 10099002, 07099002, 351455, 01109004, 10099008, 07099006, 03109005, CH-8180, 10099004, 11099002, 08099010, 09099001 and 39 more |
| Date | Nov 18, 2011 |
| 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