International safety notice
Lot Recall for Habib Bipolar Resection Device, ANGIODYNAMICS
Germany / BfArM · DEU · Nov 30, 2010
Key facts
| Title | Lot Recall for Habib Bipolar Resection Device, ANGIODYNAMICS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Habib Bipolar Resection Device, ANGIODYNAMICS |
| Manufacturer | Lot Recall for Habib Bipolar Resection Device, ANGIODYNAMICS |
| Models | 511830, 1056436-08-20-10-001-R, 30-AUGUST-2010, 1056436-08-20-10-OOI-R, 511829, 51808-1360, 87301031, 513519, 518-798-1360, 516914, 511820, Æ14624 and 10 more |
| Date | Nov 30, 2010 |
| 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