International safety notice
Corrective action for the Acetaminophen assay, Sekisui Diagnostics P.E.I. Inc.
Germany / BfArM · DEU · Jun 30, 2015
Key facts
| Title | Corrective action for the Acetaminophen assay, Sekisui Diagnostics P.E.I. Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Acetaminophen assay, Sekisui Diagnostics P.E.I. Inc. |
| Manufacturer | Corrective action for the Acetaminophen assay, Sekisui Diagnostics P.E.I. Inc. |
| Models | 46207UQ09, 46953UQ12, 29‐FEB‐2016, 30-SEP-2015, 2K99‐20, 1-877-4ABBOTT, 2K99-20, 46121UQ07, 31‐OCT‐2015, 30‐NOV‐2015, 29-FEB-2016, 1877‐4ABBOTT and 10 more |
| Date | Jun 30, 2015 |
| 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