International safety notice
Recall of dual pedal footswiches with SWAP mode - CPL 0509, Gebrüder MARTIN GmbH & Co. KG
Germany / BfArM · DEU · Jan 4, 2017
Key facts
| Title | Recall of dual pedal footswiches with SWAP mode - CPL 0509, Gebrüder MARTIN GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of dual pedal footswiches with SWAP mode - CPL 0509, Gebrüder MARTIN GmbH & Co. KG |
| Manufacturer | Recall of dual pedal footswiches with SWAP mode - CPL 0509, Gebrüder MARTIN GmbH & Co. KG |
| Models | 80-821-03-04, 706-190 |
| Date | Jan 4, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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