International safety notice
Batch recall of SUSI Instruments because of potential insterility, Aesculap AG
Germany / BfArM · DEU · Feb 16, 2012
Key facts
| Title | Batch recall of SUSI Instruments because of potential insterility, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of SUSI Instruments because of potential insterility, Aesculap AG |
| Manufacturer | Batch recall of SUSI Instruments because of potential insterility, Aesculap AG |
| Models | 51777013, 51785015, 51782877, FK850SU, 95-1019, 51774516, 51776696, 51778180, 51783056, 51782776, 51782777, 51774526 and 35 more |
| Date | Feb 16, 2012 |
| 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