International safety notice
Recall RP/VARD/20 and RP/VARD/35, MEDEX
Germany / BfArM · DEU · May 15, 2008
Key facts
| Title | Recall RP/VARD/20 and RP/VARD/35, MEDEX |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall RP/VARD/20 and RP/VARD/35, MEDEX |
| Manufacturer | Recall RP/VARD/20 and RP/VARD/35, MEDEX |
| Models | 72277, 31278, 43227, 40075, QT016, 70525, 53439, 50988, 51886, 32975, 70775, 51315 and 153 more |
| Date | May 15, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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