International safety notice
Recall of monitor cable EV2-000086 (EinsteinVision 3D-Endoscopy Systems), Schölly Fiberoptic GmbH / Aesculap AG
Germany / BfArM · DEU · Jan 31, 2017
Key facts
| Title | Recall of monitor cable EV2-000086 (EinsteinVision 3D-Endoscopy Systems), Schölly Fiberoptic GmbH / Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of monitor cable EV2-000086 (EinsteinVision 3D-Endoscopy Systems), Schölly Fiberoptic GmbH / Aesculap AG |
| Manufacturer | Recall of monitor cable EV2-000086 (EinsteinVision 3D-Endoscopy Systems), Schölly Fiberoptic GmbH / Aesculap AG |
| Models | 9321-580, 3D-ENDOSCOPY, EV2000086, 9321-566, 79208, EV.000047, 25-JAN-2017, 78532, 79211, 31701, 908-380, EV2-000086 and 1 more |
| Date | Jan 31, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 10–99 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