Instrumentation Laboratory Co.: Medical Device Recalls in 2018

According to to data from the FDA, there were 2 medical device recalls made by Instrumentation Laboratory Co. in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 - Product Usage - HemosIL¿ ReadiPlasTin is an in vitro diagnostic thromboplastin reagent, based on recombinant human tissue factor, for the quantitative determination, in human citrated plasma, of Prothrombin Time (PT) and Fibrinogen, on the ACL TOP¿ Family of analyzers. The product is intended to be used for the evaluation of the extrinsic coagulation pathway and the monitoring of Oral Vitamin K Antagonist Therapy.
• Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400