International safety notice
Lot recall of EcoPort compact F8, A.M.I. Agency for Medical Innovations GmbH / A.M.I. Deutschland GmbH
Germany / BfArM · DEU · Jan 9, 2017
Key facts
| Title | Lot recall of EcoPort compact F8, A.M.I. Agency for Medical Innovations GmbH / A.M.I. Deutschland GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Medical Innovations GmbH / A.M.I. Deutschland GmbH |
| Manufacturer | Lot recall of EcoPort compact F8, A.M.I. Agency for Medical Innovations GmbH / A.M.I. Deutschland GmbH |
| Models | 86159, 28.11.2016, 201611, 16L6629, 2016-0712, DE-86159, BYLADEM1AUG, CPS6241, 176676V, 16L6103, DE813228170, 25.10.2016 and 7 more |
| Date | Jan 9, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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