International safety notice
Corrective Action for OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH
Germany / BfArM · DEU · Jun 22, 2015
Key facts
| Title | Corrective Action for OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH |
| Manufacturer | Corrective Action for OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH |
| Models | N65P-1, 959-0, 20.05.15, DE119996067, DE19721700070252918800, N65-1, DEUTDEMM721, 252918800, 93333, 959-155, N-560, D-93333 |
| Date | Jun 22, 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