International safety notice
Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation
Germany / BfArM · DEU · Jul 31, 2006
Key facts
| Title | Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation |
| Manufacturer | Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation |
| Models | W35952, W37292, W38340, W35522, W37567, 0721-9445-129, W40410, XD10775003, W38342, W38975, 03-06, W35719 and 11 more |
| Date | Jul 31, 2006 |
| 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