MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-09-22 for JERON 680 manufactured by Jeron Electronics.
[4923424]
Code blue button testing failed - did not announce the code blue. No harm to pt. Testing was also done on 2 additional code buttons that also failed. No harm to pts.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5038350 |
| MDR Report Key | 4121859 |
| Date Received | 2014-09-22 |
| Date of Report | 2014-09-22 |
| Date of Event | 2014-09-19 |
| Date Added to Maude | 2014-09-29 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | JERON |
| Generic Name | CALL SYSTEM-CODE BLUE BUTTON |
| Product Code | ILQ |
| Date Received | 2014-09-22 |
| Model Number | 680 |
| ID Number | AGE 6 MONTHS |
| Operator | HEALTH PROFESSIONAL |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | JERON ELECTRONICS |
| Manufacturer Address | CHICAGO IL 60660 US 60660 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-09-22 |