International safety notice
Corrective action for Precision 500D, Precision Rxi and Precision MPi X-ray imaging systems (Single and dual LCD monitor suspensions), GE Healthcare
Germany / BfArM · DEU · Jul 8, 2015
Key facts
| Title | Corrective action for Precision 500D, Precision Rxi and Precision MPi X-ray imaging systems (Single and dual LCD monitor suspensions), GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Precision 500D, Precision Rxi and Precision MPi X-ray imaging systems (Single and dual LCD monitor suspensions), GE Healthcare |
| Manufacturer | Corrective action for Precision 500D, Precision Rxi and Precision MPi X-ray imaging systems (Single and dual LCD monitor suspensions), GE Healthcare |
| Models | 615451SUMRF2, 909CH500D, 609599RFP4, 770991RF1, 514326RXI, 229P503D, 801807RM3, 479441P500C, 802775MPI, 920568MPI, HC3225XR13, 417862MCRF and 767 more |
| Date | Jul 8, 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