International safety notice
Recall/Corrective Action of Beckman Coulter for Estrone RIA kit, Beckman Coulter
Germany / BfArM · DEU · Aug 24, 2010
Key facts
| Title | Recall/Corrective Action of Beckman Coulter for Estrone RIA kit, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Estrone RIA kit, Beckman Coulter |
| Manufacturer | Recall/Corrective Action of Beckman Coulter for Estrone RIA kit, Beckman Coulter |
| Models | 10020SA, 10U09RA, 100205R.A, 2010-03-17, 2010-07-13, 992630, 448-4848, PCA-13702, 100115A, 55318-1084, 2010-05-12, DSL-8700 and 16 more |
| Date | Aug 24, 2010 |
| 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