International safety notice
Recall of manual hand crank on the manual drive for Sarns™ Modular Perfusion Systems 8000, for Sarns™ Perfusion Systems 9000 and Sarns™ Centrifugal System from Terumo Cardiovascular Systems
Germany / BfArM · DEU · Mar 15, 2007
Key facts
| Title | Recall of manual hand crank on the manual drive for Sarns™ Modular Perfusion Systems 8000, for Sarns™ Perfusion Systems 9000 and Sarns™ Centrifugal System from Terumo Cardiovascular Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Sarns™ Perfusion Systems 9000 and Sarns™ Centrifugal System from Terumo Cardiovascular Systems |
| Manufacturer | Recall of manual hand crank on the manual drive for Sarns™ Modular Perfusion Systems 8000, for Sarns™ Perfusion Systems 9000 and Sarns™ Centrifugal System from Terumo Cardiovascular Systems |
| Models | 0800-115226, 164268, 16406, 0800-0222810, 808-80701, 0800-908793, 0800-293711, 0800-9179659, J1240V, 020-791373, 164290, 800-12270 and 12 more |
| Date | Mar 15, 2007 |
| 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