International safety notice
Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis
Germany / BfArM · DEU · May 30, 2016
Key facts
| Title | Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis |
| Manufacturer | Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis |
| Models | 17259055, PC0620XCE, 17290952, 17339530, 17321488, 17282142, 17265888, 17364566, 17383951, 17287347, 17295227, 17300219 and 184 more |
| Date | May 30, 2016 |
| 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