International safety notice
Recall of the Clearview Simplify D-Dimer from Unipath
Germany / BfArM · DEU · May 10, 2007
Key facts
| Title | Recall of the Clearview Simplify D-Dimer from Unipath |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Clearview Simplify D-Dimer from Unipath |
| Manufacturer | Recall of the Clearview Simplify D-Dimer from Unipath |
| Models | PT03IA, PN30A, ETAI18, 682-024„, 835003, V-.K44, 505285, 682-024, 01234, 505258, 011234, PT030A |
| Date | May 10, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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