FDA Adverse Event Malfunction Summary report: N

VACUETTE 4ML K2E K2EDTA NR LIL/S 13X75

MDR report key: 10848199 · Received November 16, 2020

Report

Report Number
1125230-2017-00016
Event Type
Malfunction
Date Received
November 16, 2020
Report Date
November 16, 2020
Manufacturer
GREINER BIO-ONE NA INC.
Product Code
JKA
PMA / PMN Number
K971236
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

COMPLAINT (B)(4). RECEIVED 50PC 454209/B17063C8 FOR EVALUATION. WE HAVE NO FURTHER COMPLAINTS ON THE MATERIAL/BATCH. WE HAVE NO FURTHER INVENTORY OF THE MATERIAL/BATCH. SAMPLES WERE TESTED, ACCORDING TO GBO STANDARD TESTING PROCEDURES, WITH REGARDS TO CORRECT ASSEMBLY, LEVEL MARK, FILLING LEVEL, AND DRAW VOLUME ACCORDING TO ISO 6710 'SINGLE USE CONTAINERS FOR VENOUS BLOOD SPECIMEN COLLECTION' AND CLSI GP39-A6 REGULATIONS FOR 'EVACUATED TUBES AND ADDITIVES FOR BLOOD SPECIMEN COLLECTION'. TUBES WERE VERIFIED TO BE CORRECTLY ASSEMBLED AND HAD THE CORRECT FILL GUIDE LINE POSITION. GREINER FILL MARK PROVIDES A VISUAL CONTROL OPPORTUNITY FOR THE PHLEBOTOMIST AND FOR THE LAB PERSONNEL TO CHECK FOR PROPER VOLUME COLLECTION OF SPECIMEN. BOTH STANDARDS SPECIFY THE DRAW VOLUME TO BE WITHIN +/- 10% RANGE OF THE NOMINAL FILL VOLUME. NO VISUAL DEVIATION IN FILL VOLUME, SPORADIC LOW OR HIGH FILL, COULD BE OBSERVED IN THE TESTED SAMPLES. ALL TUBES TESTED FILLED WITHIN THE +/-10% TOLERANCE RANGE. NO SHORT FILLS COULD BE OBSERVED ON THE SAMPLES. THE COMPLAINT COULD NOT BE CONFIRMED.

Description of Event or Problem · 1

CUSTOMER STATES TUBES ARE UNDERFILLING. THIS HAS OCCURRED ONCE WITH TWO TUBES FROM THIS LOT; 1 PHLEBOTOMIST, USING A STRAIGHT NEEDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1314540 VACUETTE 4ML K2E K2EDTA NR LIL/S 13X75 EVACUATED BLOOD COLLECTION TUBE JKA GREINER BIO-ONE NA INC. 454209 B17063C8

Patients

Seq Age Sex Outcome Treatment
1