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