PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Centurion Medical Products
Supplier initiated recall of the GRIPPER Needles
Medical equipment, implants, and diagnostic devices
Centurion Medical Products
Supplier initiated recall of the GRIPPER Needles
The product labels (pouch and carton) for products contain an incorrect value in millimeters (0.036mm) for the Guidewire Outer Diameter dimension. The inches dimension (0.014in) on the label is correct. The correct values are 0.014in (0.36mm). 0.036mm represents a typographical error.
NIBP valve assembly board subject to this recall includes enhancements that are not included in the current marketing clearance:1. Anti-motion feature 2. NIBP hose blockage identification function
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
There is a potential for Medtronic programmer and remote monitoring software applications to display an inaccurate remaining longevity estimate for a subset of implanted cardiac device models. This issue does not impact device functionality.
The product labels (pouch and carton) for products contain an incorrect value in millimeters (0.036mm) for the Guidewire Outer Diameter dimension. The inches dimension (0.014in) on the label is correct. The correct values are 0.014in (0.36mm). 0.036mm represents a typographical error.
Binding can occur between the attachment bolt and intramedullary nail, which may lead to delays in surgical procedures.
NIBP valve assembly board subject to this recall includes enhancements that are not included in the current marketing clearance:1. Anti-motion feature 2. NIBP hose blockage identification function
Becton Dickinson & Company
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Centurion Medical Products
Supplier initiated recall of the GRIPPER Needles
Valeritas, Incorporated
There is a potential for "No Needle Demo Units" to contain a needle.
Valeritas, Incorporated
There is a potential for "No Needle Demo Units" to contain a needle.
LABSTYLE INNOVATIONS
The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may experience duplicate logging of a blood glucose level reading.
The product labels (pouch and carton) for products contain an incorrect value in millimeters (0.036mm) for the Guidewire Outer Diameter dimension. The inches dimension (0.014in) on the label is correct. The correct values are 0.014in (0.36mm). 0.036mm represents a typographical error.
The contract sterilizer did not have adequate packaging data to support the 2-year shelf life.
Intuitive Surgical
The firm has identified the potential for a silicone particle to be generated within the Suction Irrigator device. If generated, a particle may be introduced into the patient with irrigation.
Centurion Medical Products
Supplier initiated recall of the GRIPPER Needles
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
There is a potential for Medtronic programmer and remote monitoring software applications to display an inaccurate remaining longevity estimate for a subset of implanted cardiac device models. This issue does not impact device functionality.
Alto Development
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
NIBP valve assembly board subject to this recall includes enhancements that are not included in the current marketing clearance:1. Anti-motion feature 2. NIBP hose blockage identification function
The product labels (pouch and carton) for products contain an incorrect value in millimeters (0.036mm) for the Guidewire Outer Diameter dimension. The inches dimension (0.014in) on the label is correct. The correct values are 0.014in (0.36mm). 0.036mm represents a typographical error.