MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-12-18 for VACUTAINER SAFETY LOCK 367297 manufactured by Becton Dickinson & Co..
[153863]
After drawing pt's blood paramedic attempted to close safety lock device over needle. He met with extreme resistance and entire buterfly twisted in his hand resulting in a needle stick.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1015258 |
| MDR Report Key | 202635 |
| Date Received | 1998-12-18 |
| Date of Report | 1998-12-18 |
| Date of Event | 1998-08-03 |
| Date Added to Maude | 1998-12-22 |
| 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 |
| Reporter Occupation | PARAMEDIC |
| 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 | VACUTAINER SAFETY LOCK |
| Generic Name | BLOOD COLLECTION DEVICE |
| Product Code | KST |
| Date Received | 1998-12-18 |
| Model Number | NA |
| Catalog Number | 367297 |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 196835 |
| Manufacturer | BECTON DICKINSON & CO. |
| Manufacturer Address | ONE BECTON DR. FRANKLIN LAKES NJ 074171880 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1998-12-18 |