International safety notice
Corrective action for the Puritan Bennett™ 980 Series Ventilator System (Universal and Neonatal Models), Covidien LLC
Germany / BfArM · DEU · Aug 25, 2015
Key facts
| Title | Corrective action for the Puritan Bennett™ 980 Series Ventilator System (Universal and Neonatal Models), Covidien LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Puritan Bennett™ 980 Series Ventilator System (Universal and Neonatal Models), Covidien LLC |
| Manufacturer | Corrective action for the Puritan Bennett™ 980 Series Ventilator System (Universal and Neonatal Models), Covidien LLC |
| Models | 959-0, PB980, 252918800, DE19721700070252918800, 93333, DEUTDEMM721, DE119996067, 959-155, 14.08.2015, D-93333 |
| Date | Aug 25, 2015 |
| 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