MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-02-11 for BD VACUTAINER URINE COMPLETE CUP KIT REF 364957 BD VACUTAINER URINE COMPLETE CUP KIT * manufactured by Becton Dickinson.
[1716505]
Needle stick: the nurse was collecting an urine sample and noticed the rubber covered end of the collection device appeared bent and was not draining. She assumed the inner portion was plastic and tried to bend it straight. Her hands were gloved, the inner portion of the device was metal.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1988343 |
| MDR Report Key | 1988343 |
| Date Received | 2011-02-11 |
| Date of Report | 2011-02-11 |
| Date of Event | 2011-02-09 |
| Report Date | 2011-02-11 |
| Date Reported to FDA | 2011-02-11 |
| Date Added to Maude | 2011-02-15 |
| 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 |
| 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 | BD VACUTAINER URINE COMPLETE CUP KIT |
| Generic Name | URINE CUP |
| Product Code | LIO |
| Date Received | 2011-02-11 |
| Model Number | REF 364957 BD VACUTAINER URINE COMPLETE CUP KIT |
| Catalog Number | * |
| Lot Number | 0302220 |
| ID Number | * |
| Device Availability | N |
| Device Age | 1 DY |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECTON DICKINSON |
| Manufacturer Address | ONE BECTON DR. FRANKLIN LAKES NJ 07417 US 07417 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-02-11 |