International safety notice
Recall for Hydrolift insertion instrument with Hydrolift hydraulic pipe, Aesculap AG
Germany / BfArM · DEU · Feb 26, 2010
Key facts
| Title | Recall for Hydrolift insertion instrument with Hydrolift hydraulic pipe, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Hydrolift insertion instrument with Hydrolift hydraulic pipe, Aesculap AG |
| Manufacturer | Recall for Hydrolift insertion instrument with Hydrolift hydraulic pipe, Aesculap AG |
| Models | 21060, 2010-02-02, 00036, 78501, 65109852, 726261, FW453802, 07461-95, FW453R, 78532 |
| Date | Feb 26, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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