MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1995-07-19 for DISPOSABLE PRESSURE TRANSDUCER 33-3X3 manufactured by Baxter Healthcare Corp..
[13548]
The red port on the dpt would not zero while the other ports would zero. Connections were checked, and no problems were noted. No pt injury or intervention.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 24664 |
MDR Report Key | 24664 |
Date Received | 1995-07-19 |
Date of Report | 1995-05-26 |
Date Added to Maude | 1995-08-18 |
Event Key | 0 |
Report Source Code | User Facility 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 | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DISPOSABLE PRESSURE TRANSDUCER |
Generic Name | PRESSURE TRANSDUCER |
Product Code | BXO |
Date Received | 1995-07-19 |
Model Number | 33-3X3 |
Lot Number | 5P16N-0876 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Age | * |
Implant Flag | N |
Date Removed | B |
Device Sequence No | 1 |
Device Event Key | 25042 |
Manufacturer | BAXTER HEALTHCARE CORP. |
Manufacturer Address | SANTA ANA CA 927111150 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1995-07-19 |