International safety notice
Recall of Remel Europe for Wellcogen Bacterial Antigen Kit
Germany / BfArM · DEU · Dec 21, 2004
Key facts
| Title | Recall of Remel Europe for Wellcogen Bacterial Antigen Kit |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Wellcogen Bacterial Antigen Kit |
| Manufacturer | Recall of Remel Europe for Wellcogen Bacterial Antigen Kit |
| Models | HW130859602, 690919, HW1308S9602, HW130858801, 20720, 890919, 20710, 20310, S-DEZ-2DD4, S-DEZ-2EE4 |
| Date | Dec 21, 2004 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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