International safety notice
Recall for BD Anaesthesia Kits and Epidural Filter, Becton Dickinson
Germany / BfArM · DEU · Oct 24, 2008
Key facts
| Title | Recall for BD Anaesthesia Kits and Epidural Filter, Becton Dickinson |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BD Anaesthesia Kits and Epidural Filter, Becton Dickinson |
| Manufacturer | Recall for BD Anaesthesia Kits and Epidural Filter, Becton Dickinson |
| Models | 249895, 249893, 173737, 176373, 401506, 256435, 149059, 201779, 158863, 230657, 173738, 273119 and 293 more |
| Date | Oct 24, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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