International safety notice
Recall and corrective action for Coulter LH 500 Hematology Analyzer PN 178832, 178833 und 178834, Beckman Coulter
Germany / BfArM · DEU · May 10, 2006
Key facts
| Title | Recall and corrective action for Coulter LH 500 Hematology Analyzer PN 178832, 178833 und 178834, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter LH 500 Hematology Analyzer PN 178832, 178833 und 178834, Beckman Coulter |
| Manufacturer | Recall and corrective action for Coulter LH 500 Hematology Analyzer PN 178832, 178833 und 178834, Beckman Coulter |
| Models | 178834, 800-526-7604, 178832, 178833, 1-800-526-7694, PUST0INER |
| Date | May 10, 2006 |
| 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