International safety notice
Corrective Action for Automated Hematology Analyzer XP-300, Sysmex
Germany / BfArM · DEU · Apr 8, 2013
Key facts
| Title | Corrective Action for Automated Hematology Analyzer XP-300, Sysmex |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Automated Hematology Analyzer XP-300, Sysmex |
| Manufacturer | Corrective Action for Automated Hematology Analyzer XP-300, Sysmex |
| Models | XP-300, POCH-100I, F3085, 13.0G, F1827, A1001, B1677, 12345-678, 10000, B1826, 15000, A2103 and 2 more |
| Date | Apr 8, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 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