International safety notice
Corrective action for Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter
Germany / BfArM · DEU · Dec 17, 2013
Key facts
| Title | Corrective action for Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter |
| Manufacturer | Corrective action for Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter |
| Models | 723585, 6605632, 429189, 21920-2, 429182, 00353, A85570, 01494, 429184, A90728 |
| Date | Dec 17, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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