MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-02-20 for * manufactured by *.
[21066694]
The cap came off a urine cup while in transit. Most of specimen leaked into the bio bag.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 4735608 |
MDR Report Key | 4735608 |
Date Received | 2015-02-20 |
Date of Report | 2015-02-20 |
Date of Event | 2015-02-11 |
Report Date | 2015-02-20 |
Date Reported to FDA | 2015-02-20 |
Date Reported to Mfgr | 2015-04-29 |
Date Added to Maude | 2015-04-29 |
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 | 3 |
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 | * |
Generic Name | CONTAINER, SPECIMINE, NON-STERILE |
Product Code | NNI |
Date Received | 2015-02-20 |
Model Number | * |
Catalog Number | * |
Lot Number | * |
ID Number | * |
Device Availability | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | * |
Manufacturer Address | * * * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-02-20 |