DiaSorin is issuing an urgent medical device correction for the LIAISON¿ Estradiol II Gen assay. Due to the risk of a recently identified cross reactivity, the LIAISON¿ Estradiol II Gena assay should not be used to test patients being treated with fulvestrant (Faslodex).
All Recalls
95,089 total recalls in our database
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
Synthes Flexible Shaft, Orthopedic manual surgical instrument The Flexible shafts are intended for use as an optional reaming step in intramedullary nailing systems.
Synthes (USA) Products
Non-conforming material used.
Pentax is initiating the product correction of several model numbers of Pentax's Colonoscope that were shipped between the clearance date of April 2014 and September 2015 because they contain the operation and reprocessing IFU's that were in use prior to the 2014 clearances and therefore did not include the cleared operation IFU, the updated reprocessing IFU or the dedicated reprocessing adaptor (for applicable models).
Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
Merit Medical Systems
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile
Synthes (USA) Products
The peel pouches for the affected reaming rods and extraction hooks are delaminating.
Waste Management Kit. Catalog Number K10-04381AP
Merit Medical Systems
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
The Hemotherm 400CE 115v, containing power board p/n 39945
Cincinnati Sub-Zero Products
The device may not maintain water flow or temperature control.
Philips Healthcare System X-ray Tomography Computed :
Philips Electronics North America
It was discovered the patient support tabletop may fail to move in the horizontal direction when it is commanded to do so during CT scans due to a potential mechanical linkage failure.
Breach in sterile barrier compromising product sterility
Product was found to contain excess residual levels of hydrogen peroxide.
Fluid Management Set. Catalog Number K08-MP5159A
Merit Medical Systems
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT system with an 40-row detector. High-speed rotation allows rapid data acquisition and shortens scan times, while the fast reconstruction unit further improves throughput, reducing the time required for diagnosis.
Toshiba American Medical Systems
Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system because it has been reported that the cooling oil in the x-ray tube heat exchanger may leak during system operation.
2.5 mm Reaming Rod with Ball Tip & Extension/950 mm, Sterile
Synthes (USA) Products
The peel pouches for the affected reaming rods and extraction hooks are delaminating.
2.5 mm TI Calibrated Reaming Rod 850 mm, Sterile
Synthes (USA) Products
The peel pouches for the affected reaming rods and extraction hooks are delaminating.
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
3.0 mm Reaming Rod/950 mm w/straight Ball Tip, Sterile
Synthes (USA) Products
The peel pouches for the affected reaming rods and extraction hooks are delaminating.