FDA Adverse Event Malfunction Summary report: N

VACUETTE TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 13X75

MDR report key: 11764274 · Received May 3, 2021

Report

Report Number
1125230-2021-00044
Event Type
Malfunction
Date Received
May 3, 2021
Report Date
May 3, 2021
Manufacturer
GREINER BIO-ONE NA INC.
Product Code
GIM
PMA / PMN Number
K971221
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

COMPLAINT STATEMENT (B)(4): A DATE OF THE EVENT COULD NOT BE OBTAINED FROM THE CUSTOMER. RECEIVED 1RK 454322/B20063QU FOR EVALUATION. NO SAMPLES OF THE OTHER CLAIMED BATCH WERE RECEIVED FOR EVALUATION. WE HAVE NO FURTHER INVENTORY OF THE MATERIAL/BATCHES. 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 GUIDELINE 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. THE COMPLAINT COULD NOT BE DUPLICATED.

Description of Event or Problem · 1

CUSTOMER STATES 2 LOTS OF TUBES ARE UNDERFILLING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
663809 VACUETTE TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 13X75 EVACUATED BLOOD COLLECTION TUBE GIM GREINER BIO-ONE NA INC. 454322 B2005378, B20063QU

Patients

Seq Age Sex Outcome Treatment
1