International safety notice
QIAGEN
United Kingdom / MHRA · GBR · Nov 18, 2021
Key facts
| Title | QIAGEN |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | QIAcube Connect MDx |
| Manufacturer | QIAGEN |
| Models | PROM-19631-001, DNA_QIAAMPDSPDNABLOODMINI_WHOLEBLOOD_ELUTIONVOLUME100_V1, VIRUS_QIAAMPDSPVIRALRNA_BODYFLUID_MANUALLYSIS_V1, DNA_QIAAMPDSPDNABLOODMINI_WHOLEBLOOD_ELUTIONVOLUME200_V1, DNA_QIAAMPDSPDNAMINI_BACTERIALPELLET_BACTERIALDNA_V1, DNA_QIAAMPDSPDNAMINI_BLOODORBODYFLUID_STANDARD_V1, VIRUS_QIAAMPDSPVIRUSSPIN_PLASMAORSERUM_STANDARD_V2, ORYEAST_ENZYMATICLYSIS_V1, VIRUS_QIAAMPDSPVIRUSSPIN_PLASMAORSERUM_MANUALLYSIS_V2, VIRUS_QIAAMPDSPVIRALRNA_BODYFLUID_STANDARD_V1, _BLOOD_PAXGENEBLOODRNAPARTAANDB_V4, 9003070 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Nov 18, 2021 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes 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