MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-01 for BD VACUTAINER? URINE COLLECTION CUPS 364975 manufactured by Becton, Dickinson & Co..
[134899064]
Date of event: unknown. The date received by manufacturer has been used for this field. Device expiration date: unknown. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed. Device manufacture date: unknown.
Patient Sequence No: 1, Text Type: N, H10
[134899145]
It was reported that after use of the bd vacutainer urine collection cup there was leakage while transporting urine cup.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1917413-2019-00161 |
MDR Report Key | 8299338 |
Date Received | 2019-02-01 |
Date of Report | 2019-02-11 |
Date of Event | 2019-01-13 |
Date Mfgr Received | 2019-01-13 |
Date Added to Maude | 2019-02-01 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | BDX BRETT WILKO |
Manufacturer Street | 9450 SOUTH STATE STREET |
Manufacturer City | SANDY UT 84070 |
Manufacturer Country | US |
Manufacturer Postal | 84070 |
Manufacturer Phone | 8015652341 |
Manufacturer G1 | BECTON, DICKINSON & CO. |
Manufacturer Street | 150 SOUTH 1ST AVENUE |
Manufacturer City | BROKEN BOW NE 68822 |
Manufacturer Country | US |
Manufacturer Postal Code | 68822 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | BD VACUTAINER? URINE COLLECTION CUPS |
Generic Name | SPECIMEN TRANSPORT AND STORAGE CONTAINER |
Product Code | KDT |
Date Received | 2019-02-01 |
Catalog Number | 364975 |
Lot Number | UNKNOWN |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON, DICKINSON & CO. |
Manufacturer Address | 150 SOUTH 1ST AVENUE BROKEN BOW NE 68822 US 68822 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-02-01 |