International safety notice
Corrective action for APTIMA Urine Collection Kit, Hologic Deutschland GmbH / Gen-Probe Incorporated
Germany / BfArM · DEU · Jun 12, 2014
Key facts
| Title | Corrective action for APTIMA Urine Collection Kit, Hologic Deutschland GmbH / Gen-Probe Incorporated |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | APTIMA Urine Collection Kit, Hologic Deutschland GmbH / Gen-Probe Incorporated |
| Manufacturer | Corrective action for APTIMA Urine Collection Kit, Hologic Deutschland GmbH / Gen-Probe Incorporated |
| Models | 5891635, 7076155, 27232, 27234, 65205, 27231, 301040, 301040-01, 27233 |
| Date | Jun 12, 2014 |
| 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