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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls
Class I - Dangerous

Potential for the Connectivity Engine Module of the affected unit to disengage from the main chassis, causing the unit to shut down without an alarm notification. This would delay initiation of therapy or interrupt an infusion.

Jun 15, 2017 Infusion Pumps Nationwide View Details →

Signa PET/MR (K163619, K142098) Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information, acquired simultaneously and isocentrically. The combined system maintains independent functionality of the MR and PET devices, allowing for single modality MR and/or PET imaging. These systems are intended to be utilized by appropriately trained health care professionals to aid in the detection, localization, and diagnosis of diseases and disorders. The MR is intended to produce transverse, sagittal, coronal and oblique cross-sectional MR images, spectroscopic images and/or spectra, and displays the internal structure and/or function of the human body. Other physical parameters derived from the images and/or spectra may also be produced. Depending on the region of interest, approved contrast agents may be used, as described in their labeling. This system may also be used for imaging during interventional procedures when performed with MR compatible devices, such as MR safe biopsy needles. The PET images and measures the distribution of PET radiopharmaceuticals in humans to aid the physician in determining various metabolic (molecular) and physiologic functions within the human body for evaluation of diseases and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer. The combined system utilizes the MR for radiationfree attenuation correction maps for PET studies. The system provides inherent anatomical reference for the fused PET and MR images due to precisely aligned MR and PET image coordinate systems.

GE Medical Systems

Class I - Dangerous

Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.

May 11, 2017 Diagnostic Equipment Nationwide View Details →

Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.

May 11, 2017 Implants & Prosthetics Nationwide View Details →

LeadCare II Test Kits controls out of range

Jan 20, 2016 Diagnostic Equipment Nationwide View Details →

Insufficient documentation to support product sterility claims.

Jun 23, 2017 Surgical Instruments Nationwide View Details →

Insufficient documentation to support product sterility claims.

Jun 23, 2017 Surgical Instruments Nationwide View Details →