International safety notice
Batch recall of DOLPHIN inflation device, PEROUSE MEDICAL / Vygon
Germany / BfArM · DEU · May 2, 2017
Key facts
| Title | Batch recall of DOLPHIN inflation device, PEROUSE MEDICAL / Vygon |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of DOLPHIN inflation device, PEROUSE MEDICAL / Vygon |
| Manufacturer | Batch recall of DOLPHIN inflation device, PEROUSE MEDICAL / Vygon |
| Models | 0185QL, CL3030, R1703879, 1612XXXX, 0185NA, 0185PD, 1504XXXX, 34408, CARDI0V.SERVCLIENT, 0185ND, 317883, 1601XXXX and 9 more |
| Date | May 2, 2017 |
| 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