Emerging Venture Catheters Recall Litigation
A Class 1 FDA Recall has been issued by the FDA related to certain Catheters manufactured by Venture Solutions, Inc. between 2015 and 2017.
FDA Communication Excerpt:
“Vascular Solutions, Inc. is recalling the Venture catheter because there is a risk of the catheter tip splitting or separating during use. Excess material at the tip of the catheter may separate and could enter the patient’s bloodstream. This can result in serious adverse health consequences such as the development of blood clots, embolism of the excess material to vital organs, or death”
Learn More About the Emerging Venture Catheters Recall Litigation
The emerging Venture Catheters Recall will be used as a case study in the May 18-21, 2018 Mass Tort Nexus, “Four Days to Mass Tort Success Course” To register for the May Course, contact Jenny Levine at firstname.lastname@example.org or call (954) 520-4494.
For information on the class and to enroll, use this link-“Enroll Here To Attend “Four Days to Mass Tort Success”
Course attendees will receive the benefit of a step by step analysis of the emerging Venture Catheters Recall Litigation using these primary metrics:
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