MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2001-08-10 for OHMEDA 22F122M * manufactured by Ohmeda.
[18191383]
Pt intubated. Anesthesia machine being moved by anesthesiologist when flow transducer broke. It required force to remove the broken pieces at the connections. Once it was removed, the flow transducer was replaced with a new one.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1022600 |
| MDR Report Key | 346425 |
| Date Received | 2001-08-10 |
| Date of Report | 2001-08-07 |
| Date of Event | 2001-08-06 |
| Date Added to Maude | 2001-08-14 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | OHMEDA |
| Generic Name | FLOWTRANSDUCER |
| Product Code | BXP |
| Date Received | 2001-08-10 |
| Model Number | 22F122M |
| Catalog Number | * |
| Lot Number | 113136 |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 335742 |
| Manufacturer | OHMEDA |
| Manufacturer Address | 616 SIX FLAGS DR, STE 310 ARLINGTON TX 76011 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2001-08-10 |