International safety notice
Recall for the Allura Xper FD R8.2.1.1, Philips Medical Systems
Germany / BfArM · DEU · Dec 15, 2015
Key facts
| Title | Recall for the Allura Xper FD R8.2.1.1, Philips Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Allura Xper FD R8.2.1.1, Philips Medical Systems |
| Manufacturer | Recall for the Allura Xper FD R8.2.1.1, Philips Medical Systems |
| Models | 722034, 722028, 722033, 722036, 21CFR1020.32, XCR603-150608, 722058, 722039, ÄCN-2000206, 722038, MA-FC072200327, 60601 and 12 more |
| Date | Dec 15, 2015 |
| 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