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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Diagnostic Equipment Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Diagnostic Equipment Nationwide View Details β†’

A software issue was discovered where an inaccurate FFR/iFR value could be calculated under certain circumstances.

Jun 22, 2015 Diagnostic Equipment Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Diagnostic Equipment Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sure flex'" Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Diagnostic Equipment Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex'" Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Surgical Instruments Nationwide View Details β†’

Product marketed without a 510(k)

Jul 6, 2015 Surgical Instruments Nationwide View Details β†’

Potential for the Balseal, a small wire spring coil located on the post feature of the ATTUNE Knee Tibial Articulation Surface Instruments used in trialing to become damaged and disassociate (come off). If the Balseal is separated from the post, it has the potential to enter the surgical site and be left in the patient if the surgeon is unaware of the disassociation.

Jun 12, 2015 Implants & Prosthetics Nationwide View Details β†’

A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.

Jun 12, 2015 Diagnostic Equipment Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex'" Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Surgical Instruments Nationwide View Details β†’

Philips has identified four (4) software defects in the Tumor LOC software application that may potentially result in irradiation of healthy tissue or non-irradiation of diseased tissue.

Jul 1, 2015 Diagnostic Equipment Nationwide View Details β†’

Philips has identified four (4) software defects in the Tumor LOC software application that may potentially result in irradiation of healthy tissue or non-irradiation of diseased tissue.

Jul 1, 2015 Diagnostic Equipment Nationwide View Details β†’

The firm has become aware of the possibility of ignition and rupture (explosion) of a compressed gas oxygen cylinder, which can cause serious injury and/or death.

Jan 31, 2015 Other Medical Devices View Details β†’

System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP and ADVIA Centaur/ADVIA Centaur XP/ADVIA Centaur XPT systems.

May 19, 2015 Diagnostic Equipment Nationwide View Details β†’

Devon Light Gloves contain splits or holes compromising the sterility

Apr 16, 2015 Surgical Instruments Nationwide View Details β†’

validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex'" Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products

May 28, 2015 Surgical Instruments Nationwide View Details β†’

Philips has identified four (4) software defects in the Tumor LOC software application that may potentially result in irradiation of healthy tissue or non-irradiation of diseased tissue.

Jul 1, 2015 Diagnostic Equipment Nationwide View Details β†’