Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong blade. The box contains Myringotomy Spear Blade (Juvenile).
Other Medical Devices
🏥 Medical Devices • 15,809 recalls
CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials.
NeuraWrap Nerve Protector NeuraWrap Nerve Protector is indicated for the management of peripheral nerve injuries in which there has been no substantial loss of nerve tissue.
Integra LifeSciences
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
Segmented Cylinder Applicator Set, Model # GM11004150, when used for Pulsed Dose Rate (PDR) Product Usage: Usage: Used during pulsed dose rate brachytherapy to treat vaginal and rectal cancer.
Varian Medical Systems
Segmented cylinder applicator set may slip during treatment, causing the delivery of radiation to areas outside the target.
NeuraGen Nerve Guide NeuraGen Nerve Guide is indicated for repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
Integra LifeSciences
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
Absorbable Collagen Sponge Provided As Intermediate to Another Company
Integra LifeSciences
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
Varian High Energy Clinacs, High Energy Accelerator, Radiation Treatment System, Model Numbers: H14, H27, H29, HCX. Product Usage: The Varian High Energy Accelerator is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.
Varian Medical Systems, Inc. Oncology Systems
Under certain conditions, photon beams in High Energy Clinacs may experience a gradual change in beam symmetry, potentially reaching an asymmetry of up to about 7% before interlock occurs. At maximum asymmetry, this may result in no more than about 3.5% dose deviation from expected at any point in the beam, and may result in minor injury to the patient or slightly decreased local disease control.
On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
Presource PBDS, Shoulder Procedure, Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Presource PBDS, Shoulder Arthroscopy, Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Codman(R) Collins Radioparent Sternal Blade Nylon,4 3/4" (121 mm) long, 3" (76 mm) wide, 1 1/2" (38 mm) deep, REF 50-8081 sternum retractor
Symmetry Medical/SSI
There is a possibility that the Collins Radioparent Sternal Blades Nylon may break during use.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
ExoShape Soft Tissue Fastener 12 mm x 30 mm REF 1101-00-1230. For use in the fixation of ligaments, tendons or soft tissue grafts to bone.
Medshape Solutions
Expiration date on the patient label and date on the product carton were not the same.
Presource PBDS, Hand, Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.