International safety notice
Smith Medical recalls the Portex Spinal Epidural Needle Sets
Germany / BfArM · DEU · Apr 27, 2006
Key facts
| Title | Smith Medical recalls the Portex Spinal Epidural Needle Sets |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Smith Medical recalls the Portex Spinal Epidural Needle Sets |
| Manufacturer | Smith Medical recalls the Portex Spinal Epidural Needle Sets |
| Models | 484785, 102141, 484797, 102140, 487515, 493491, 487391, 100Ι396Ι916, 102139, 488099, 488098, 396Ι916 and 62 more |
| Date | Apr 27, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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