International safety notice
Corrective Action for SYNCHRON Systems Phenobarbital (PHE) Reagent, Beckman Coulter
Germany / BfArM · DEU · Sep 28, 2009
Key facts
| Title | Corrective Action for SYNCHRON Systems Phenobarbital (PHE) Reagent, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | SYNCHRON Systems Phenobarbital (PHE) Reagent, Beckman Coulter |
| Manufacturer | Corrective Action for SYNCHRON Systems Phenobarbital (PHE) Reagent, Beckman Coulter |
| Models | SYNCHRON_M807743, 29.0-41.0, M810083, M902320, 45.0-71, 469600, SYNCHRON_M802293, SYNCHRON_M807742, 29.5-41, M810440, SYNCHRON_M802292, M902272 and 8 more |
| Date | Sep 28, 2009 |
| 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