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Catheters depend on their tubing and connections holding up under repeated access, and a fracture, leak, or blockage can interrupt treatment or introduce a serious complication.
At The Law Offices of Sean M. Cleary, we look closely at the specific catheter involved to determine whether a defect contributed to what you experienced.
Case EvaluationA catheter system generally includes the tubing itself, a connection point, and in the case of a port, a septum used for access, and each part carries its own risk.
Several manufacturers have issued corrections tied to specific catheter and port models in recent years, often affecting a particular lot or configuration rather than an entire product line.
These examples happen to involve Bard products, but recalls affecting catheters and implanted ports have come from other manufacturers as well, including B. Braun, Teleflex, and AngioDynamics.
Some of these problems are noticed immediately during a clinic visit, while others only become clear on a later scan.
A failed catheter can add a whole separate course of treatment on top of whatever condition it was placed to manage.
Because catheter recalls often apply to a specific lot, catalog number, or configuration, matching your exact device against manufacturer and FDA records is typically where a case review starts. The Law Offices of Sean M. Cleary works through your implant card and medical records to make that comparison. There is no cost to speak with us, and our fee only applies if your case results in compensation. If a catheter or implanted port has fractured, migrated, or caused an infection, get in touch and tell us what your doctors have found so far.