International safety notice
Recall for the Allura Xper ED R2.x, Philips Medical Systems
Germany / BfArM · DEU · Dec 14, 2015
Key facts
| Title | Recall for the Allura Xper ED R2.x, Philips Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Allura Xper ED R2.x, Philips Medical Systems |
| Manufacturer | Recall for the Allura Xper ED R2.x, Philips Medical Systems |
| Models | MA-FC072200287, 1-800-722-9377, 722006, XCN-2000206, 722124, 020.32, 60601-2-54, 203.6.2.1, CFR1020.32, 606012-54, FC072200287, XCR603-150623 |
| Date | Dec 14, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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