International safety notice
Recall of PROPAQ LT Patient Monitors from WelchAllyn
Germany / BfArM · DEU · Mar 20, 2007
Key facts
| Title | Recall of PROPAQ LT Patient Monitors from WelchAllyn |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of PROPAQ LT Patient Monitors from WelchAllyn |
| Manufacturer | Recall of PROPAQ LT Patient Monitors from WelchAllyn |
| Models | 001940, KA001647, KA002460, 002192, 002777, WELCHA11YN, 001651, KA002161, 001960, 001969, KA001703, 001655 and 54 more |
| Date | Mar 20, 2007 |
| 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