International safety notice
Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland
Germany / BfArM · DEU · Jun 4, 2007
Key facts
| Title | Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland |
| Manufacturer | Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland |
| Models | 22934VM, 10.DOC, 20721VM, 26573VM, 29957VM, 21752VM, 26702VM, 32241VM, 33428VM, 23166VM |
| Date | Jun 4, 2007 |
| 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