BD VACUTAINER® LITHIUM HEPARINN (LH) 37 USP UNITS BLOOD COLLECTION TUBES
Report
- Report Number
- 1917413-2018-01851
- Event Type
- Malfunction
- Date Received
- June 12, 2018
- Date of Event
- May 9, 2016
- Report Date
- May 13, 2019
- Manufacturer
- BECTON, DICKINSON & CO.
- Product Code
- JKA
- UDI-DI
- 50382903666640
- PMA / PMN Number
- K901449
- Removal / Correction Number
- PAS-18-1175-FA
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
ADDITIONAL INFORMATION: BD IS ISSUING A VOLUNTARY MEDICAL DEVICE CORRECTION FOR BD VACUTAINER® PLASTIC LITHIUM HEPARIN TUBES. FALSE ELEVATION OF CARBOXYHEMOGLOBIN (COHB) RESULTS HAVE BEEN REPORTED WHEN ANALYZING VENOUS BLOOD SAMPLES COLLECTED WITH BD VACUTAINER® PLASTIC LITHIUM HEPARIN TUBES WITH THE IL GEM 4000 INSTRUMENT. PLEASE REFERENCE BD RECALL #: PAS-18-1175-FA.
IT WAS REPORTED THAT BD VACUTAINER® LITHIUM HEPARINN (LH) 37 USP UNITS BLOOD COLLECTION TUBES HAD "ERRONEOUS RESULTS." NO SERIOUS INJURY OR MEDICAL INTERVENTION.
BD RECEIVED SAMPLES FROM THE CUSTOMER FACILITY FOR INVESTIGATION. THE SAMPLES WERE EVALUATED AND THE CUSTOMER'S INDICATED FAILURE MODE WITH THE INCIDENT LOT WAS NOT OBSERVED. A REVIEW OF THE MANUFACTURING RECORDS WAS COMPLETED FOR THE INCIDENT LOT AND NO ISSUES WERE IDENTIFIED.
IT WAS REPORTED THAT BD VACUTAINER® LITHIUM HEPARIN (LH) 37 USP UNITS BLOOD COLLECTION TUBES HAD "ERRONEOUS RESULTS." NO SERIOUS INJURY OR MEDICAL INTERVENTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 436270 | BD VACUTAINER® LITHIUM HEPARINN (LH) 37 USP UNITS BLOOD COLLECTION TUBES | BLOOD SPECIMEN COLLECTION DEVICE | JKA | BECTON, DICKINSON & CO. | 5154680 | 50382903666640 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |