MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-10-10 for GASTROCCULT * 6286604037 manufactured by Beckman Coulter.
[2285524]
Gastroccult strips were reading hemoglobin positive before testing solution was placed on the strips. The test was done 3 times on 3 different strips using the same patient gastric content.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2300337 |
| MDR Report Key | 2300337 |
| Date Received | 2011-10-10 |
| Date of Report | 2011-10-10 |
| Date of Event | 2011-10-05 |
| Report Date | 2011-10-10 |
| Date Reported to FDA | 2011-10-10 |
| Date Added to Maude | 2011-10-19 |
| 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 | GASTROCCULT |
| Generic Name | GASTROCCULT |
| Product Code | KHE |
| Date Received | 2011-10-10 |
| Model Number | * |
| Catalog Number | 6286604037 |
| Lot Number | * |
| ID Number | * |
| Operator | NURSE |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECKMAN COULTER |
| Manufacturer Address | 606 ELMWOOD AVE. SHARON HILL PA 19079 US 19079 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-10-10 |