International safety notice
Lot recall of Quo-Test A1C Test Kit, EKF-diagnostic GmbH
Germany / BfArM · DEU · Jun 20, 2016
Key facts
| Title | Lot recall of Quo-Test A1C Test Kit, EKF-diagnostic GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of Quo-Test A1C Test Kit, EKF-diagnostic GmbH |
| Manufacturer | Lot recall of Quo-Test A1C Test Kit, EKF-diagnostic GmbH |
| Models | 00000209600600, 00000118625300, 31.12.2016, 101939, 020279, 233820, HR3101939, 020301, 511414, 3ARLEBEN, 810100000118625300, EKF062016 and 4 more |
| Date | Jun 20, 2016 |
| 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