Zilver PTX Stent Recall Issued Due to Tip Separation Risk
All Zilver PTX drug eluting stents have been recalled due to a faulty delivery system, which may not meet government standards, resulting in at least one patient death and other…
All Zilver PTX drug eluting stents have been recalled due to a faulty delivery system, which may not meet government standards, resulting in at least one patient death and other…
Federal health officials have ordered hospitals to remove several lots of Guardian II hemostasis valves from their inventory because they could cause patients to suffer a deadly air embolism.
Reports of problems involving leaks and disconnections have led to a recall of Covidien’s size 8 Shiley tracheostomy tubes.
Federal health regulators are warning that defects with the Inspira AIR balloon dilation system could lead to patient deaths.
Alabama health officials are investigating nine deaths that may be linked to contaminated nutritional supplements by Med IV, an Alabama compounding pharmacy.
A Class 1 medical device recall has been issued for Transseptal Sheath Introducer Kits by Thomas Medical Products, a subsidiary of General Electric’s healthcare division, because the sheath tips can…
The FDA has issued a Class 1 recall for several models of Baxter HomeChoice automated dialysis systems because of a defect that can cause the machines to overfill a patient’s…
A Class 1 medical device recall has been issued for Safesheath CSG Sheath Introducer Systems by Thomas Medical Products, Inc. due to reports that the tip of the sheath can break…
A recall has been issued for 17 different types of Portex pediatric tracheal tubes due to a potential defect that could cause some of the tubes to have internal diameters…
The FDA released a warning letter yesterday that was sent to C.R. Bard, Inc. regarding “adulterated” medical products manufactured at their plant in Puerto Rico, which is where the company…