MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-04-15 for LABOR ASSEMBLY BAR manufactured by Hill-rom Co., Inc..
[9265]
Used labor bar to assist with pushing. Radial palsies were noted immediately after.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1001603 |
| MDR Report Key | 12764 |
| Date Received | 1994-04-15 |
| Date of Event | 1994-02-20 |
| Date Added to Maude | 1994-04-19 |
| 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 | LABOR ASSEMBLY BAR |
| Generic Name | LABOR ASSEMBLY BAR (SQUAT BAR) |
| Product Code | HHP |
| Date Received | 1994-04-15 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 12764 |
| Manufacturer | HILL-ROM CO., INC. |
| Manufacturer Address | BATESVILLE IN 47006 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 1994-04-15 |