International safety notice
Corrective action for Ambu Silicone Plus Resusciators from the manufacturer Ambu
Germany / BfArM · DEU · Aug 4, 2006
Key facts
| Title | Corrective action for Ambu Silicone Plus Resusciators from the manufacturer Ambu |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ambu Silicone Plus Resusciators from the manufacturer Ambu |
| Manufacturer | Corrective action for Ambu Silicone Plus Resusciators from the manufacturer Ambu |
| Models | 87826, 87731, 87838, 87765, DK-2750, 87812, 63644919, 87842, 87839, 87643, 87896, 040085 and 16 more |
| Date | Aug 4, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers 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