BEUDAMED
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    Hemochron Jr. Whole Blood Microcoagulation system Low Range Activated Clotting Time. ACT-LR Cuvettes. In vitro diagnostic use, non-sterile, Packaged in individual foil pouches. 45 foil pouches per shelf carton box. Mfg. by International Technidyne Corp, Edison, NJ 08820.

    FDA Recall
    Terminated ·International Technidyne Corp.·Product code JBP·April 27, 2005

    Celite ACT Cartridge Cartridge is useful for monitoring patients receiving heparin for treatment of pulmonary embolism or venous thrombosis, and for monitoring anticoagulation therapy in patients undergoing medical procedures such as catheterization, cardiac surgery, surgery organ transplantation and dialysis.

    FDA Recall
    Terminated ·Abbott Point Of Care Inc.·Product code JBP·December 3, 2010

    Abbott i-STAT ACT Kaolin Cartridges. In vitro diagnostic test which uses fresh whole blood to monitor high-dose heparin anticoagulation frequently associated with cardiovascular surgery.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JBP·August 18, 2009

    Item # 4042-CPR Rescue Kit, containing CPR shield with one way valve & barrier filter. brand Lifeline, UPC 845174004429 each; UPC 845174004436 master case of 6. Item #4043-CPR Rescue Kit, containing CPR shield with one way valve & barrier filter. brand Lifeline. UPC Red color kit: 845174005464; UPC Lime color kit: 845174005594; UPC Purple color: 845174005600; UPC of master case of 6 845174005471 (2 each color) Item # 4037, Outfitter First Aid Kit, CPR shield with one way valve & barrier filter, brand Lifeline, UPC 845174003453

    FDA Recall
    Terminated ·Lifeline First Aid LLC·Product code CBP·May 16, 2016

    i-STAT Celite ACT Cartridge. ACT, activated clotting time, celite activated clotting time test.

    FDA Recall
    Terminated ·Abbott Laboratories·Product code JBP·March 16, 2005

    One Way Valve/Female to Male Flow, 22 mm I.D./22 mm O.D., Ref 396798, Lot ***, SINGLE USE ONLY, Latex Free, Quantity 50 Each Manufactured for and Distributed by RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098, Made in Taiwan.

    FDA Recall
    Terminated ·Rusch Inc·Product code CBP·February 3, 2004

    Abbott i-STAT ACT Celite Cartridges. In vitro diagnostic test used to monitor moderate and high-level heparin therapy through analysis of arterial and venous whole blood samples.

    FDA Recall
    Terminated ·Abbott Point of Care Inc.·Product code JBP·August 18, 2009

    Hemochron Jr. ACT- LR Assay (JACT- LR); ITC Catalogue/Code Number: JACTLR 45 Cuvettes; For Performance on the HEMOCHROM Whole Blood Microagulation Systems; International Technidyne Corp., Edison, NJ 08820. The HEMOCHRON Jr. ACT-LR is a quantitative assay for monitoring heparin anticoagulation during various medical procedures. The ACT-LR demonstrated linear correlation to the anticoagulation effects of heparin up to 2.5 unit/ml of blood. It is intended for use in monitoring low to moderate heparin doses frequently associated with procedures such as cardiac catheterization, Extracorporeal Membrane Oxygenation (ECMO) Hemodialysis, and Percutaneous Transluminal Coronary Angioplasty.

    FDA Recall
    Terminated ·International Technidyne Corp.·Product code JBP·May 5, 2009

    CPR Shield With One Way Valve and Barrier Filter, Reorder No. 4921 --- Dynarex label, 100 per case --- Manufactured for: Dynarex Corporation - Made in China. Used as a physical barrier for mouth to mouth resuscitation.

    FDA Recall
    Terminated ·Dynarex Corporation·Product code CBP·July 2, 2014

    5195GM, Cadillac First Aid Kit, #23459698, brand General Motors. No UPC.

    FDA Recall
    Terminated ·Lifeline First Aid LLC·Product code CBP·May 16, 2016

    i-STAT ACT Kaolin Cartridges in vitro diagnostic test which uses fresh whole blood to monitor high-dose heparin anticoagulation frequently associated with cardiovascular surgery.

    FDA Recall
    Terminated ·Abbott Point Of Care Inc.·Product code JBP·October 6, 2010

    Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code JBP·October 20, 2025

    One Way Valve/Male to Female Flow, 22 mm I.D./22 mm O.D., Ref 396799, Lot ***, SINGLE USE ONLY, Latex Free, Quantity 50 Each Manufactured for and Distributed by RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098, Made in Taiwan.

    FDA Recall
    Terminated ·Rusch Inc·Product code CBP·February 3, 2004

    4-Way Tee with 2 one-way valves, Ref 395945 Lot***, SINGLE USE ONLY, Qty 1 ea, RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098***. Carton labeling was similar to individual unit labeling, except for, ***Qty 50 ea.

    FDA Recall
    Terminated ·Rusch Inc·Product code CBP·February 3, 2004