FDA Adverse Event Other Summary report: N

SST BRAND TUBE

MDR report key: 244876 · Received October 12, 1999

Report

Report Number
1024879-1999-00020
Event Type
Other
Date Received
October 12, 1999
Date of Event
September 13, 1999
Report Date
October 11, 1999
Manufacturer
BECTON DICKINSON & CO.
Product Code
JKA
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

TOP OF TUBE BROKE WHEN RE-INSERTING STOPPER BACK INTO BLOOD COLLECTION TUBE, CAUSING TECH. TO CUT HER FINGER WHICH REQUIRED (2) STITCHES. BASELINE TESTING AND HIV COCKTAIL GIVEN AS PER FACILITY POLICY. SOURCE BLOOD TESTED POSITIVE FOR HBD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SST BRAND TUBE SST TUBE JKA BECTON DICKINSON & CO. NA 9C901

Patients

Seq Age Sex Outcome Treatment
1 NA