International safety notice
Recall for ACCUPROBE Group B Streptococcus kit, ACCUPROBE Mycobacterium tuberculosis Complex kit and ACCUPROBE Mycobacterium avium Complex kit, Gen-Probe
Germany / BfArM · DEU · Jan 27, 2009
Key facts
| Title | Recall for ACCUPROBE Group B Streptococcus kit, ACCUPROBE Mycobacterium tuberculosis Complex kit and ACCUPROBE Mycobacterium avium Complex kit, Gen-Probe |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ACCUPROBE Group B Streptococcus kit, ACCUPROBE Mycobacterium tuberculosis Complex kit and ACCUPROBE Mycobacterium avium Complex kit, Gen-Probe |
| Manufacturer | Recall for ACCUPROBE Group B Streptococcus kit, ACCUPROBE Mycobacterium tuberculosis Complex kit and ACCUPROBE Mycobacterium avium Complex kit, Gen-Probe |
| Models | 554524, 555096, 858-410-8250, 554864, 554076, 556421, 555170, 2820F, 555167, 554628, 556204, 554840 and 12 more |
| Date | Jan 27, 2009 |
| 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