International safety notice
Corrective action and recall for Coulter LH 700 und Gen•S Haematology analyzers, Beckman
Germany / BfArM · DEU · Jan 19, 2006
Key facts
| Title | Corrective action and recall for Coulter LH 700 und Gen•S Haematology analyzers, Beckman |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter LH 700 und Gen•S Haematology analyzers, Beckman |
| Manufacturer | Corrective action and recall for Coulter LH 700 und Gen•S Haematology analyzers, Beckman |
| Models | 6605360, 16-9015, 147TH, 6605381, 83196-2500, T47TH, 526-6932, 6605470, 33196-2500, 169015, OPERATOR9, 526-7694 and 6 more |
| Date | Jan 19, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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