ITC-Nexus Dx Recalls
3 recalls on record · November 13, 2013 to July 30, 2014 · Medical Devices
Recalls by year
13
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 30, 2014Medical DevicesFDA
ITC-Nexus Dx recalls Hemochron Jr. Whole Blood Microcoagulation System APTT Cuvette. For in vitro diagnostic coagulation test. Catalog numbe
Hazard: Test results may be erroneously elevated or report an out-of-range high (OOR-H) error code in non heparinized blood samples.
February 12, 2014Medical DevicesFDA
ITC-Nexus Dx recalls Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized microcoagulation test intended to be used in performing a
Hazard: ITC has determined that some Citrate APTT cuvettes may recover higher than expected results in normal individuals.
November 13, 2013Medical DevicesFDA
ITC-Nexus Dx recalls Surgicutt fully automated incision making device for bleeding time determination. ITC 8 Olsen Avenue, Edison, NJ 08820
Hazard: ITC has determined that the blade in their Surgicutt with Blotting Paper (Product Code: SUB50I; Lot: AK301M) devices may be loose.