International safety notice
Corrective action for Freelite Serum Free Light Chain Assays of The Binding Site
Germany / BfArM · DEU · Jul 25, 2006
Key facts
| Title | Corrective action for Freelite Serum Free Light Chain Assays of The Binding Site |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Freelite Serum Free Light Chain Assays of The Binding Site |
| Manufacturer | Corrective action for Freelite Serum Free Light Chain Assays of The Binding Site |
| Models | 3.30-19.40MG, 0.26-1.65, 1866-06, 5.71-26.30MG, 11712, V2.DOC |
| Date | Jul 25, 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