International safety notice
LeMaitre recalls the Pruitt Aortic Occlusion Catheter
Germany / BfArM · DEU · Jun 16, 2005
Key facts
| Title | LeMaitre recalls the Pruitt Aortic Occlusion Catheter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | LeMaitre recalls the Pruitt Aortic Occlusion Catheter |
| Manufacturer | LeMaitre recalls the Pruitt Aortic Occlusion Catheter |
| Models | BLDG65812, 1030404-09, 1052204-01, 2105-15, 1061404-04, 2120-12, 1070204-03, 00604-01, 2-9-4, 221-2266, 20768800, 1010505-08 and 26 more |
| Date | Jun 16, 2005 |
| 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