International safety notice
Lot recall of NuPortCT and C-PortCT port catheter systems containing F9.6 silicone catheters, PHS Medical GmbH
Germany / BfArM · DEU · Feb 17, 2017
Key facts
| Title | Lot recall of NuPortCT and C-PortCT port catheter systems containing F9.6 silicone catheters, PHS Medical GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of NuPortCT and C-PortCT port catheter systems containing F9.6 silicone catheters, PHS Medical GmbH |
| Manufacturer | Lot recall of NuPortCT and C-PortCT port catheter systems containing F9.6 silicone catheters, PHS Medical GmbH |
| Models | 2017-02-02, PH-096IS-CA, BASO4, 02.02.2017, A1635008, 14.09.2016, 01606081, RKL036, 19.10.2016, 34277, 49-561-99, A1639003 and 8 more |
| Date | Feb 17, 2017 |
| 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