Lawsuit Alleges Bard PowerPort Failure Led to Deep Vein Thrombosis Injuries
A Bard PowerPort lawsuit claims the drug access port both failed and caused deep vein thrombosis in a patient's neck.
Interested in the Bard PowerPort lawsuit?
Tag Archives: Catheter
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Bard PowerPort Lawsuit Filed Over Catheter Bloodstream Infection
A Bard PowerPort lawsuit claims a defectively designed catheter has led to a woman's catheter bloodstream infection, as well as numerous other complications in other patients.
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Arrow MAC Venous Catheter Kit Recall Issued Over Risk of Leaks, Bleeding and Death
The FDA has given the Arrow MAC catheter kit recall a class I designation, meaning it poses a risk of serious injury or death to patients.
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Medtronic Palindrome and Mahurkar Catheter Recall: Defect Could Cause Serious Injury or Death
More than 1 million Medtronic hemodialysis catheters are being recalled due to the risk of leaks which could cause severe injuries or patient deaths.
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Abbott Dragonfly OpStar Catheter Recall Issued Over Tip Separation Risks
A Dragonfly OpStar Imaging Catheter recall was announced after reports of tip separations.
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Medtronic Harmony Delivery Catheter Recall Issued Following Reports of Capsule Breaking
Medtronic is recalling hundreds of Harmony Delivery Catheters due to a risk of separated tips, patient injuries and deaths.
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Medtronic TurboHawk Catheter Recall Issued Due to Tips Breaking
The FDA has given a class I designation to a recall of Medtronic TurboHawk atherectomy systems due to a risk of the catheter tips breaking off and causing life-threatening arterial…
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Medtronic HawkOne Directional Atherectomy System Recall Issued Over Broken Tip Risks
Medtronic is recalling more than 95,000 HawkOne Directional Atherectomy Systems whose catheter tips could break off, putting patients' lives at risk.
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Do Not Use ChloraPrep 3 mL Applicators Due to Microbial Contamination Risk, FDA Warns
The FDA is warning against the use of certain BD ChloraPrep applicators due to the risk of microbial contamination and infections.
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Cook Medical Flexor Catheter Recall Following Reports of Serious Injuries
A Cook Medical Catheter recall has been given class I status by the FDA following dozens of injuries which occurred when weak bonding sites separated during surgery.
