International safety notice
Recall of specific lots of the EnVision™ FLEX/HRP visualization reagent, Dako
Germany / BfArM · DEU · Oct 9, 2015
Key facts
| Title | Recall of specific lots of the EnVision™ FLEX/HRP visualization reagent, Dako |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of specific lots of the EnVision™ FLEX/HRP visualization reagent, Dako |
| Manufacturer | Recall of specific lots of the EnVision™ FLEX/HRP visualization reagent, Dako |
| Models | 20022298, 20019097, CAPA00544, 20020773, 20017712, DM822, 20020785, K8023, 20018510, 20021381, 20020777, K8024 and 34 more |
| Date | Oct 9, 2015 |
| 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