International safety notice
Safety Corrective Action/Recall for PORT-A-CATH® Plastic Hub Needles, Smiths Medical
Germany / BfArM · DEU · Sep 21, 2015
Key facts
| Title | Safety Corrective Action/Recall for PORT-A-CATH® Plastic Hub Needles, Smiths Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | PORT-A-CATH® Plastic Hub Needles, Smiths Medical |
| Manufacturer | Safety Corrective Action/Recall for PORT-A-CATH® Plastic Hub Needles, Smiths Medical |
| Models | 55112, 212287-24, 21-2287-24, 46262, 21-2005-24 |
| Date | Sep 21, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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