International safety notice
Recall/Corrective Action for Coulter HmX and HmX AL Hematology Analyzers and for Coulter MAXM and MAXM AL Hematology Analyzers, Beckman Coulter
Germany / BfArM · DEU · Feb 2, 2011
Key facts
| Title | Recall/Corrective Action for Coulter HmX and HmX AL Hematology Analyzers and for Coulter MAXM and MAXM AL Hematology Analyzers, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter MAXM and MAXM AL Hematology Analyzers, Beckman Coulter |
| Manufacturer | Recall/Corrective Action for Coulter HmX and HmX AL Hematology Analyzers and for Coulter MAXM and MAXM AL Hematology Analyzers, Beckman Coulter |
| Models | 33196-2500, 6605525, 6605526, 123456, 6705999, 6705996, 147TH, 6605524, 6705998, 526-6932, 6604569, 6705995 and 16 more |
| Date | Feb 2, 2011 |
| 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