MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2018-10-05 for GIRAFFE OMNIBED CARESTATION 2082844-001 manufactured by Ohmeda Medical.
[122851037]
Ge healthcare's investigation into the reported occurrence is still ongoing. A follow-up report will be issued when the investigation has been completed. Device evaluation anticipated, but not yet begun.
Patient Sequence No: 1, Text Type: N, H10
[122851038]
It was reported to ge healhcare that a baby was placed in the unit. At some point, the baby was found to be on the floor. There were reportedly no witnesses. As a result of the fall, the infant had an extended hospital stay due to a subdural hematoma on the side of the head.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1121732-2018-00008 |
| MDR Report Key | 7938511 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2018-10-05 |
| Date of Report | 2018-11-09 |
| Date of Event | 2018-08-17 |
| Date Mfgr Received | 2018-10-17 |
| Device Manufacturer Date | 1970-01-01 |
| Date Added to Maude | 2018-10-05 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | JOHN SZALINSKI |
| Manufacturer Street | 3000 N GRANDVIEW BLVD. |
| Manufacturer City | WAUKESHA WI |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | GIRAFFE OMNIBED CARESTATION |
| Generic Name | INCUBATOR, NEONATAL |
| Product Code | FMZ |
| Date Received | 2018-10-05 |
| Model Number | 2082844-001 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OHMEDA MEDICAL |
| Manufacturer Address | 8880 GORMAN RD LAUREL, MD 20723 US 20723 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2018-10-05 |