Louisiana recalls

Philips identified that some Allura Xper FD20 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete previous service work. If the tray is not installed, coolant can leak onto electrical components and cause a short circuit, potentially shutting down the system.

Philips identified that some Allura Xper FD10/10 X-ray systems may be missing a drip tray that protects electrical components from coolant liquid. If the tray was not installed during a previous service, coolant could contact electrical parts and cause a short circuit, potentially shutting down the system.

Philips identified that in 56 X-ray systems worldwide, a drip tray beneath the cooling unit may not have been installed during previous maintenance, or the installation may not have been properly documented. If missing, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.

Philips has identified that 18 Allura Xper FD20 Biplane X-ray systems worldwide may be missing a drip tray beneath the cooling unit due to incomplete field repairs or missing documentation. Without this tray, coolant liquid could contact electrical components and cause short circuits that shut down the system.

Philips identified that some Allura Xper FD20 X-ray systems may be missing a drip tray beneath the cooling unit from previous service work. Without this tray, coolant could leak onto electrical components and cause a short circuit, potentially shutting down the system during use.

Philips identified that 14 of their Allura Xper FD10/10 X-ray systems may be missing a drip tray beneath the cooling unit. Without this tray, coolant liquid could contact electrical parts and cause a short-circuit, potentially shutting down the system.

Philips identified that some Allura Xper FD10 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete field repairs. If the tray is not in place, coolant can leak onto electrical components and cause short-circuits, potentially shutting down the system.

Philips identified that some Allura Xper FD10F imaging systems may be missing a drip tray beneath the cooling unit due to incomplete field corrections. If the drip tray is not in place, coolant liquid could contact electrical components and cause short-circuits, potentially shutting down the system.

Philips has identified that some Allura Xper FD10C X-ray systems may be missing a drip tray that sits beneath the cooling unit, or the installation was not properly documented during previous maintenance. Without this tray, coolant liquid could leak onto electrical components and cause short circuits, potentially shutting down the system.

BD Ready-to-Use Hydrophilic Catheters (14 Fr, straight tip, model RTU14F) distributed in Georgia have an incorrect expiration date printed on the label. This labeling error means the actual shelf life of the product may differ from what is shown. No injuries have been reported.

Medline surgical kits containing B. Braun IV Administration Sets have been recalled because the check valve components may become stuck in the open or closed position. This could affect fluid flow during medical procedures. The recall affects four specific surgical kit types distributed nationwide.

Medline kits containing B. Braun IV administration sets have been recalled because the check valve components may become stuck in either the open or closed position. This could affect proper fluid delivery through the IV line. The affected kits are labeled as Neuro Angio Pack with SKU DYNJ38935, lot number 25IBC144.

Medline kits containing B. Braun IV Administration Sets may have check valve components that can become stuck in the open or closed position. This could affect proper fluid delivery during IV administration. About 1,725 units are affected nationwide.

Medline pre-op kits containing B. Braun IV administration sets have been recalled because the check valve components inside can get stuck in either the open or closed position. This could affect proper fluid delivery during medical procedures. No injuries have been reported to date.

Medline has recalled five IV starter kits that contain B. Braun IV administration sets. The check valve components in these sets may become stuck in the open or closed position, which could affect proper IV fluid delivery. No injuries have been reported so far.

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline kits labeled DR HOLCOMB FACIAL PACK (SKU DYNJ54488A) contain B. Braun IV Administration Sets with check valve components that may become stuck in the open or closed position. This can prevent proper fluid flow during IV administration. The recall affects 16 units distributed nationwide.

Medline kits containing B. Braun IV Administration Sets have been recalled because the check valve components may get stuck in either the open or closed position. This could affect how medication or fluids flow through the IV line. No injuries have been reported, but the sets should not be used.

Medline surgical kits containing B. Braun IV administration sets may have check valve components that become stuck in the open or closed position. This could affect fluid delivery during medical procedures. About 96 kits are affected.

Medline Deluxe Pre Op Kits containing B. Braun IV Administration Sets may have check valve components that stick in the open or closed position. This could affect the proper flow of intravenous fluids during medical procedures. The issue affects specific lot numbers distributed nationwide.

Medline has recalled eight models of cardiac surgery kits that contain B. Braun IV administration sets. The check valve components in these sets may become stuck in either the open or closed position, which could affect fluid delivery during surgery. No injuries have been reported.

Medline kits containing B. Braun IV administration sets have been recalled because the check valve components may become stuck in the open or closed position. This could prevent proper fluid flow during medical procedures. The recall affects 10 units distributed nationwide.

Fresenius Kabi is issuing a recall for the Ivenix Infusion System (IIS) with LVP Software version 5.10.2 and earlier. The manufacturer is emphasizing instructions for LVP duration programming in the device manual to ensure proper use. No injuries have been reported.

GE HealthCare identified that certain older GE MAXXUS Nuclear Medicine systems may have been moved or transported without proper detector support. This could damage the detector mounting and potentially cause the detector to fall, which poses a serious injury risk. No injuries or detector falls have been reported so far.

GE HealthCare identified that certain older SMV BodyTrack nuclear medicine systems may have been moved or transported without proper detector support during their service life. This can weaken the detector mounting mechanisms. If the detector becomes loose or falls, it could cause serious injury. No injuries or detector falls have been reported so far.

GE HealthCare discovered that certain older SMV DSI nuclear medicine systems may have been moved or transported without proper detector support. This can stress the detector mounting and potentially cause the detector to fall, which could injure someone. No falls or injuries have occurred yet.

GE HealthCare identified that certain older SMV DSX nuclear medicine systems may not have been properly supported during transport or relocation. This could damage the detector mounting mechanisms and potentially cause the detector to fall, creating a serious safety risk. No injuries have been reported so far.

The Vanta A71200 Clinician Programmer App (versions 2.0.2465 and 2.0.2683) running on Samsung tablets may not work properly during use. This malfunction could delay or postpone surgical procedures. The implanted neurostimulator devices themselves are not affected—only the programming software.

Boston Scientific found that certain batches of Coyote Over-the-Wire PTA Balloon Dilation Catheters may not inflate or deflate properly during use due to a manufacturing process variation. The issue affects only catheters made between September 12 and October 13, 2025. The company has corrected the manufacturing process.

Mobius Imaging's detachable 10-inch pendant upgrade kits for AIRO Computed Tomography systems are missing a required "Safe Hand Position Warning" label. This label is important for safe operation of the equipment. The affected units were distributed nationwide.