MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-08-02 for INTRAN PLUS IVP-400 manufactured by Utah Medical Products, Inc..
[17766816]
Pt was 40+ weeks in active labor. Device was inserted. It did not function properly and monitoring was inadequate. It was removed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 35797 |
| MDR Report Key | 35797 |
| Date Received | 1996-08-02 |
| Date of Report | 1996-08-01 |
| Date of Event | 1996-08-01 |
| Date Facility Aware | 1996-08-01 |
| Report Date | 1996-08-01 |
| Date Reported to FDA | 1996-08-01 |
| Date Reported to Mfgr | 1996-08-01 |
| Date Added to Maude | 1996-08-26 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| 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 | INTRAN PLUS |
| Generic Name | DISPOSABLE INTRAUTERINE PRESSURE CATHETER SYSTEM |
| Product Code | KXO |
| Date Received | 1996-08-02 |
| Model Number | IVP-400 |
| Catalog Number | IVP-400 |
| Lot Number | UNK |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | 1 DAY |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 37223 |
| Manufacturer | UTAH MEDICAL PRODUCTS, INC. |
| Manufacturer Address | 7043 S 300 WEST MIDVALE UT 84047 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1996-08-02 |