International safety notice
Extended Recall for the product ala®octa, alamedics GmbH & Co. KG
Germany / BfArM · DEU · Nov 24, 2015
Key facts
| Title | Extended Recall for the product ala®octa, alamedics GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product ala®octa, alamedics GmbH & Co. KG |
| Manufacturer | Extended Recall for the product ala®octa, alamedics GmbH & Co. KG |
| Models | 101003, 060912, 210115, 110213, 041213, 101004, 060813, 040712, 10993-5, 101001, 261112, 541800 and 23 more |
| Date | Nov 24, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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