Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
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Surgical Instruments
🏥 Medical Devices • 7,015 recalls
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.
Leica Microsystems (Schweiz) Ag
Class I - Dangerous
The brake in the Z axis and/or brakes in the AB and C axes failed during installation.
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Ormco Corporation is voluntarily recalling one lot of 8 MM Vector TAS Screws because some screws of this lot were machined undersized at the top of the threads may potentially cause a weakening of the screw. Use of the undersized product may result in breakage of the screw during insertion or removal when torqued, possibly requiring surgical removal of any remaining pieces.
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray - Drug Free may occlude, preventing drainage of excessive fluid from the pleural cavity leading to a potential delay in the medical procedure and potentially serious patient complications.
Class I - Dangerous
Baxter Healthcare Corporation is voluntarily recalling one lot of Baxa Vial Adapters, 14mm - Luer Lock, due to incorrect expiry date.
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Class I - Dangerous
Table was not lowering.
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of Small Peripheral Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilatation Devices and Flextome Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilation Devices. Boston Scientific has determined that users may experience significant difficulty or inability to remove the protector cap from the devic
Class I - Dangerous
The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk of rotation of the broth table when the door is open.
Class I - Dangerous
SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
Class I - Dangerous
The firm initiated this recall of certain lots of Illico Ti Cannulated Polyaxial Screws 7.5mm x 40mm implants, due to an off-center cannulation hole at the proximal end of the bone screw. There is a potential risk that when the screw is mated to a polyaxial screwdriver, the guide wire may not pass through the screwdriver.
Megadyne Medical Products is recalling certain lots of E-Z Clean, L-Wire laproscopic Electrode Standard Stem and Split Stem due to potential breach of insulation.
Stryker received reports of the desiccant bag in the kit leaking silica gel granulate. This could increase exposure to anesthesia during surgical delay up to 60 minutes or inadvertent implantation of silica gel granulate which could cause foreign body reaction including inflammation and might lead to the need for revision surgery.
DeRoyal Industries is recalling their product Insufflation Tubing Sets due to materials incompatibility which could possibly result in occlusion at or near the filter housing which could prevent the flow of gas through the device.