International safety notice
Recall for ala purple, alamedics GmbH & Co. KG
Germany / BfArM · DEU · Feb 5, 2016
Key facts
| Title | Recall for ala purple, alamedics GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ala purple, alamedics GmbH & Co. KG |
| Manufacturer | Recall for ala purple, alamedics GmbH & Co. KG |
| Models | 40770-0, D-89160, AV120315, AV120215, 722783, 121002, GENODEF1NUV, 541800, AV100614, 60887, AV131014, DE278235367 and 11 more |
| Date | Feb 5, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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