International safety notice
Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic
Germany / BfArM · DEU · Jul 31, 2006
Key facts
| Title | Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | intrathecal catheter model 8598 form the manufacturer Medtronic |
| Manufacturer | Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic |
| Models | 5293-109, 5293-116, 5293-171, 52703-171 |
| Date | Jul 31, 2006 |
| 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