International safety notice
Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis
Germany / BfArM · DEU · Dec 20, 2006
Key facts
| Title | Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis |
| Manufacturer | Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis |
| Models | 4193060, 3889103, 4034040, 3984040, 381602, 414705, 4313107, 4301070, 4085105, 3982040, 42720, 0641-80041 and 184 more |
| Date | Dec 20, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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