International safety notice
Recall of the Premier Edge MVR 19g Knife and the Premier Edge MVR 20g Knife from OASIS Medical
Germany / BfArM · DEU · Aug 14, 2007
Key facts
| Title | Recall of the Premier Edge MVR 19g Knife and the Premier Edge MVR 20g Knife from OASIS Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Premier Edge MVR 19g Knife and the Premier Edge MVR 20g Knife from OASIS Medical |
| Manufacturer | Recall of the Premier Edge MVR 19g Knife and the Premier Edge MVR 20g Knife from OASIS Medical |
| Models | 3520A, PE3520A, 800.528.9786, PE3519, PE3S20A, 800.S28.97GE, 626.852.5156, DK0307D, OE.08.07, 626.914.9372, 14712, DK0107Y and 14 more |
| Date | Aug 14, 2007 |
| 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