MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1995-06-12 for MILLER-ABBOTT TUBE 16FR 20 50 manufactured by Rusch, Inc..
[17245750]
Mercury containment failed, releasing hg into pt's bowel. Recovered approx 3cc from pt's bile excretion. Dr reported injecting 10 cc into tube.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1006209 |
| MDR Report Key | 22390 |
| Date Received | 1995-06-12 |
| Date of Report | 1995-05-25 |
| Date of Event | 1995-05-17 |
| Date Added to Maude | 1995-06-12 |
| 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 | MILLER-ABBOTT TUBE |
| Generic Name | MILLER-ABBOTT TUBE |
| Product Code | FEF |
| Date Received | 1995-06-12 |
| Model Number | 16FR |
| Catalog Number | 20 50 |
| Lot Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 22525 |
| Manufacturer | RUSCH, INC. |
| Manufacturer Address | DULUTH GA 30136 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1995-06-12 |