International safety notice
Lot / batch recall of ORBITARIS handle, Günter Bissinger Medizintechnik GmbH
Germany / BfArM · DEU · Mar 10, 2017
Key facts
| Title | Lot / batch recall of ORBITARIS handle, Günter Bissinger Medizintechnik GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot / batch recall of ORBITARIS handle, Günter Bissinger Medizintechnik GmbH |
| Manufacturer | Lot / batch recall of ORBITARIS handle, Günter Bissinger Medizintechnik GmbH |
| Models | 82460005, 949458, 8246000X, 948670, 032017, 948986, 82460004, DRESDEFF680, 35128, 79680800300410387700, 8246000K, 948303 and 7 more |
| Date | Mar 10, 2017 |
| 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