International safety notice
Corrective action and recall for Ortho AutoVue and AutoVue Ultra
Germany / BfArM · DEU · Apr 27, 2006
Key facts
| Title | Corrective action and recall for Ortho AutoVue and AutoVue Ultra |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ortho AutoVue and AutoVue Ultra |
| Manufacturer | Corrective action and recall for Ortho AutoVue and AutoVue Ultra |
| Models | 06-077, 06223, VERF•71SCHTE, 1817022, 08001817022, 62.23.77A, 200604-10, 06-076, 2006-04, 13.04.2006, OTTHO-CLUICA1, 6223-77-0 and 2 more |
| Date | Apr 27, 2006 |
| 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