International safety notice
Recall of Becton Dickinson for the BD ProCOUNTTM Progenitor Cell Enumeration Kit
Germany / BfArM · DEU · Aug 19, 2005
Key facts
| Title | Recall of Becton Dickinson for the BD ProCOUNTTM Progenitor Cell Enumeration Kit |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the BD ProCOUNTTM Progenitor Cell Enumeration Kit |
| Manufacturer | Recall of Becton Dickinson for the BD ProCOUNTTM Progenitor Cell Enumeration Kit |
| Models | 03-798, 340991, 12-RESULTS, IO.08.2005, 340498, 22561 |
| Date | Aug 19, 2005 |
| 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