New York recalls

Becton Dickinson has recalled certain ForeSight Elite tissue oximetry cables due to incorrect labeling of Channel 1 and Channel 2 on the module and flag labels. This labeling error could cause clinicians to misread oxygen saturation data if the cables are connected to the wrong channels. The affected cables were distributed to hospitals and healthcare facilities.

A software issue in Philips EPIQ Elite ultrasound systems (Model 795234, software version 14.0) causes doppler blood flow measurements to display at incorrect depths. This can lead to inaccurate velocity readings and potential misdiagnosis of vascular conditions. About 219 units are affected worldwide.

A small number of Pearle Vision 1 day contact lenses in one affected lot were manufactured with incorrect lens power. This could result in blurred or distorted vision if the wrong lens is worn. No injuries have been reported.

Olympus has recalled certain BiCOAG Hemostasis Probe units (Model CD-B622LA) because the ceramic tip may detach during use. This can happen because some units were manufactured without the correct amount of adhesive securing the tip. No injuries have been reported so far.

Olympus identified that certain BiCOAG Hemostasis Probe units (Model CD-B620LA) may have been manufactured with insufficient adhesive, creating a risk that the ceramic tip could detach during use. This affects all unexpired lots of this model worldwide.

Olympus is recalling certain BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector devices (model CD-B612LA) because the ceramic tip may detach during use. This can happen because some units were manufactured without the correct amount of adhesive. The issue affects 105 devices distributed worldwide, with no injuries reported to date.

Olympus has recalled the BiCOAG Hemostasis Probe (Model CD-B610LA) because the ceramic tip may detach during use. The problem stems from manufacturing that did not apply the correct amount of adhesive. This affects 404 units distributed worldwide, though no injuries have been reported.

A software issue in Philips SmartPath MRI systems can stop an examination during image reconstruction if scan parameters are manually adjusted in ways that exceed the system's available memory. This interruption may require the scan to be repeated.

A software issue in certain Philips MR 7700 MRI machines can cause an examination to stop during image reconstruction if scan parameters are manually adjusted in a way that exceeds the system's available memory. This affects 37 machines worldwide.

A software issue in certain Philips MR 5300 MRI scanners can cause the system to shut down unexpectedly during image reconstruction if scan parameters are manually adjusted in ways that exceed the scanner's available memory. This interruption stops the examination and may require the scan to be restarted.

A software issue in certain Philips Intera 1.5T MRI machines can cause an examination to stop during image processing if scan settings are manually adjusted in ways that require more memory than the system has available. This could interrupt patient scans and require them to be repeated.

A software problem in certain Philips MRI systems can cause an examination to stop unexpectedly during image reconstruction if scan settings are manually adjusted in a way that exceeds the system's available memory. This interruption may require the scan to be repeated, delaying diagnosis and treatment.

A software issue in certain Philips Ingenia 3.0T and 3.0T CX MRI machines can cause the system to stop abruptly during image reconstruction if scan parameters are manually adjusted in a way that exceeds available system memory. This interruption could require the scan to be repeated, delaying patient imaging.

Philips Ingenia Ambition S and X MRI systems contain a software issue that can cause an examination to terminate unexpectedly during image reconstruction if scan parameters are manually adjusted in certain ways. This interruption occurs when the reconstruction requirements exceed the system's available memory.

A software problem in certain Philips Ingenia 1.5T MRI machines can cause an examination to stop unexpectedly during image reconstruction if a technician manually adjusts scan parameters in a way that exceeds the system's available memory. This interruption could delay patient care and require the scan to be repeated.

Certain Philips Evolution upgrade 1.5T and 3.0T MRI systems contain a software issue that can cause an examination to terminate unexpectedly during image reconstruction. This happens when scan parameters are manually adjusted in a way that exceeds the system's available memory.

A software issue in certain Philips Achieva XR MRI scanners can cause an examination to stop abruptly during image reconstruction if scan parameters are manually adjusted in ways that exceed the system's available memory. This affects 15 devices worldwide.

A software issue in certain Philips Achieva 3.0T MRI scanners can cause an examination to terminate unexpectedly during image reconstruction if scan parameters are manually adjusted in a way that exceeds the system's available memory. This affects specific serial numbers across five model variants distributed worldwide.

A software problem in certain Philips Achieva 1.5T MRI machines can cause a scan to stop unexpectedly during image processing if technicians manually adjust scan settings in a way that requires more memory than the system has available. This affects specific serial numbers of five model variants distributed worldwide.

Some units of the Biomerieux VITEK 2 AST-N461 test kit used to determine antibiotic susceptibility in gram-negative bacteria have damaged card pouches. This damage can cause the test to report false resistant results, which may lead to use of less effective antibiotics or unnecessary antibiotic combinations.

Medline convenience kits (models DYNJ48258D and DYNJ48258F) contain Healthmark Instrument Channel Brushes with potential sharp edges or burrs on the brush ends. These sharp edges could cause cuts, abrasions, or infections during use.

Medline convenience kits (models DYNJ48258D and DYNJ48258F) contain Healthmark Instrument Channel Brushes with a potential sharp edge or burr on the brush end. This sharp edge could cause a cut, abrasion, or infection if the brush is handled or used.

SeaSpine Orthopedics is recalling certain Extended Polyaxial Head spinal implants (model MD1-300010-12) because the proximal thread depth does not meet design specifications. This defect could affect the secure attachment of the device during spinal surgery. No injuries have been reported.

Fresenius Medical Care is issuing a communication regarding its CombiSet hemodialysis blood tubing set (Model 03-2522-1) to ensure healthcare providers and patients review the product's instructions for use. The company is recommending that all treatment preparation and handling steps be performed exactly as instructed to maintain safe operation.

Maquet PowerLED 300 concealed lighting systems may detach at the connection between the spring arm and suspension arm. This could cause the device to fall and potentially injure someone in an operating room or clinical setting.

Ventec Life Systems HomeFill cylinder D oxygen products do not have the required medical gas labeling on some units. This labeling is needed to ensure safe identification and proper handling of the oxygen cylinders.

Ventec Life Systems' HomeFill Cylinder M9 units lack required medical gas labeling on the cylinders themselves. This labeling is a safety requirement that helps users and healthcare providers identify the contents and proper handling of the oxygen cylinders. Two units with specific serial numbers were affected.

Ventec Life Systems HomeFill Cylinder M9 oxygen cylinders lack required medical gas labeling on the product. These cylinders were distributed in Florida, Iowa, Ohio, Nebraska, and Tennessee. Without proper labeling, users may not have complete safety and product information.

Midmark's IQvitals Zone vital signs monitor may provide inaccurate blood pressure readings when using the Linear Deflation Method. The issue affects a limited number of units (33 total) distributed nationwide. No injuries have been reported.

Midmark Corporation's IQvitals Zone vital signs monitor may produce inaccurate blood pressure readings when using the Linear Deflation Method. The issue affects a limited number of units with specific serial numbers distributed nationwide. No injuries have been reported.