International safety notice
Recall of Active Renin IRMA Test Kit, Beckman Coulter
Germany / BfArM · DEU · Feb 17, 2012
Key facts
| Title | Recall of Active Renin IRMA Test Kit, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Active Renin IRMA Test Kit, Beckman Coulter |
| Manufacturer | Recall of Active Renin IRMA Test Kit, Beckman Coulter |
| Models | 111212C, 2012-02-10, 111114C, 2012-01-16, 1-800-854-3633, DSL25100, 55318-1084, 2011-12-16, 448-4848, PCA-18692, 2011-11-18, 111017D and 2 more |
| Date | Feb 17, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 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