FDA Adverse Event Malfunction Summary report: N

BD VACUTAINER® PLASTIC URINE COLLECTION CUP

MDR report key: 7075240 · Received December 1, 2017

Report

Report Number
1917413-2017-00204
Event Type
Malfunction
Date Received
December 1, 2017
Date of Event
April 4, 2016
Report Date
January 24, 2018
Manufacturer
BECTON, DICKINSON & CO.
Product Code
KDT
PMA / PMN Number
EXEMPT
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INITIAL MDR WAS SUBMITTED WITH THE 510K NUMBER LISTED AS K790366. IT IS CORRECTED TO READ EXEMPT.

Additional Manufacturer Narrative · 1

DATE OF EVENT: UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. MEDICAL DEVICE EXPIRATION DATE: UNKNOWN. LOT #: UNKNOWN. DEVICE MANUFACTURE DATE: UNKNOWN. RESULTS: BD RECEIVED SAMPLES FROM THE CUSTOMER FACILITY FOR INVESTIGATION. THE SAMPLES WERE EVALUATED AND THE CUSTOMER'S INDICATED FAILURE MODE FOR FOREIGN MATTER OR MOLD ON URINE CUPS WITH THE INCIDENT LOT WAS NOT OBSERVED. BD WAS UNABLE TO DETERMINE THE SPECIFIC LOT NUMBER ASSOCIATED WITH THIS COMPLAINT. THEREFORE, A REVIEW OF THE DEVICE HISTORY RECORD COULD NOT BE CONDUCTED. CONCLUSION: UNCONFIRMED COMPLAINT. AN ABSOLUTE ROOT CAUSE FOR THIS INCIDENT CANNOT BE DETERMINED AS BD WAS NOT ABLE TO DUPLICATE OR CONFIRM THE CUSTOMERS¿ INDICATED FAILURE MODE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THERE WAS AN APPEARANCE OF FOREIGN MATTER OR MOLD ON 120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUPS. NO SERIOUS INJURY, BLOOD TO MUCOUS MEMBRANE EXPOSURE OR MEDICAL INTERVENTION WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
853612 BD VACUTAINER® PLASTIC URINE COLLECTION CUP URINE COLLECTION CUP KDT BECTON, DICKINSON & CO. UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other