BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc testing in plasma for in vitro diagnostic use.
Reported: April 4, 2018 Initiated: September 18, 2017 #Z-1180-2018
Product Description
BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc testing in plasma for in vitro diagnostic use.
Reason for Recall
Increased amount of residual blood present on the top of stopper well after venipuncture
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 1,976,000 tubes
- Distribution
- USA (nationwide)
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc testing in plasma for in vitro diagnostic use.. Recalled by Becton Dickinson & Company. Units affected: 1,976,000 tubes.
Why was this product recalled? ▼
Increased amount of residual blood present on the top of stopper well after venipuncture
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1180-2018.
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