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All product recalls associated with Avid Medical Inc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Defect in packaging of medical devices may compromise sterility of these products used in medical and surgical procedures.
The recall includes Coleman® Gas Grills with model numbers 5100, 5300, 5400, 5600, 6000 and 7700, and Coleman® Patio Heater with model number 5040. The model name and number can be found directly on the front of the grills and on the inside cover of the heaters.
The pointed end of a screw securing the occluder to the delivery cable could scrape off microscopic fragments of the polytetrafluorethylene (PTFE) plastic lining of the sheath. Those shavings could potentially migrate into a patient's bloodstream.
Potential for voltage pins in connector of therapy cable to break.
Component of procedure kits may allow higher than desired amount of IV solution to be infused in to patient during pressure monitoring procedure.
Potential for voltage pins in connector of therapy cable to break.
This recall involves DesignWare® child-size sunglasses with Sesame Street character decals. Sold in quantities of four, each package contains a yellow, blue, red and green pair of sunglasses. The bright green cardboard backer has the Sesame Street and DesignWare® logo on the front, and model number SUN-1219 on the back.
Tear away sheath assembly may contain a sheath (8FR) that is not the correct French size for the dilator (7FR).
Potential compromise of sterile packaging for disposable dissecting tools.
Five lots of AMPLATZER Vascular Plugs were sterilized in a load that was not validated for the AMPLATZER Vascular Plug. However, only three of those five lots were distributed.
Customers stated that the U-Clip deployment collar was either difficult to rotate or 'locks up' during usage, which prevents the deployment of the U-Clips.
Potential Safety related problem associated with the pace detect function on some Advisor monitors that have impedance respiration capabilities in that random pace markers may appear when the pace detect function is turned on and the primary lead is set to Lead II, III or any of the augmented leads, AVL, AVR or AVF on the Advisor monitor.
Enpath has become aware that some of the Enpath Medical 8 Fr Steerable sheath devices may have non-conforming hemostasis valves in that the valve can leak or the valve was observed to have a small hole.
Two lots of J-VAC Drain Reservors were shipped to Japan prior to sterilization and were released.
The vector selector has an electrical design flaw which prevents RV pacing.
Data from internal testing indicates that the Nichols Advantage Invasive Trophoblast Antigen Assay Cartridges (ITA)(Lot No 62-500261) and Hyperglycosylated Human Chorionic Gonadotropin Assay Cartridges (H-hCG)(Lot No 62-500262) does not maintain its stability over the 12 month expiration dating of the product, and that stability is assured only through 6 months.
Data from internal testing indicates that the Nichols Advantage Invasive Trophoblast Antigen Assay Cartridges (ITA)(Lot No 62-500261) and Hyperglycosylated Human Chorionic Gonadotropin Assay Cartridges (H-hCG)(Lot No 62-500262) does not maintain its stability over the 12 month expiration dating of the product, and that stability is assured only through 6 months.
The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.
"Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues additional products are now being classified by the agency". Foreign deposit present on the surface of the Vidaurri LASIK Flap Irrigators
The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.