International safety notice
Recall of ARCHITECT CA 19-9XR (Lot-No.: 08849M500 - 08853M500, 10122M500 and 10040M500), Abbott
Germany / BfArM · DEU · Jun 11, 2012
Key facts
| Title | Recall of ARCHITECT CA 19-9XR (Lot-No.: 08849M500 - 08853M500, 10122M500 and 10040M500), Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of ARCHITECT CA 19-9XR (Lot-No.: 08849M500 - 08853M500, 10122M500 and 10040M500), Abbott |
| Manufacturer | Recall of ARCHITECT CA 19-9XR (Lot-No.: 08849M500 - 08853M500, 10122M500 and 10040M500), Abbott |
| Models | 18.01, 60064-6081, FA30MAY2012, 08849M500, 08852M500, 08853M500, 19-9XR, 2K91-20, 2K91-27, 10040M500, 2K91-25, 10122M500 and 2 more |
| Date | Jun 11, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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