International safety notice
Lot recall of application devices by SFM Medical Devices GmbH, Octapaharma
Germany / BfArM · DEU · Oct 30, 2013
Key facts
| Title | Lot recall of application devices by SFM Medical Devices GmbH, Octapaharma |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of application devices |
| Manufacturer | SFM Medical Devices GmbH, Octapaharma |
| Models | 0340‐5508, B311C120A, MIX2VIAL, 06847, «NAME4», «NAME2», 0340-5508, A308A181A, B303C120A, «NAME3», 16.07.2013, 40764 |
| Date | Oct 30, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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