International safety notice
Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax
Germany / BfArM · DEU · Nov 21, 2006
Key facts
| Title | Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax |
| Manufacturer | Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax |
| Models | 207-730-5700, 04074, 024038, 852-000, 207-730-5710, 024448, 852-430 |
| Date | Nov 21, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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