Kentucky recalls

Certain versions of Elekta's MOSAIQ oncology information system may deliver twice the intended radiation dose to cancer patients under specific conditions involving partial treatments and interrupted fields. This could occur when the system fails to verify the correct dose amount after a treatment interruption. The issue affects systems using particle therapy with certain software versions.

Philips identified that 8 Allura Xper FD20/20 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete installation or documentation during previous repairs. If the tray is not in place, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.

Philips identified that a small number of Allura Xper FD20/10 X-ray systems may be missing a drip tray that should be installed beneath the cooling unit. Without this tray, coolant liquid could contact electrical components and cause short-circuits, potentially shutting down the system.

Philips identified that in 2 Allura Xper FD20 X-ray systems, the drip tray under the cooling unit was not installed or not properly documented during previous maintenance. If missing, coolant liquid could contact electrical parts and cause a short circuit, leading to system shutdown.

Philips has identified that some Allura Xper FD10/10 X-ray systems may be missing a drip tray that was supposed to be installed beneath the cooling unit during a previous service. Without this tray, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Philips identified that in a small number of operating room tables, a drip tray beneath the cooling unit may not have been installed during previous maintenance, or the installation was not properly documented. If missing, coolant could leak onto electrical components and cause a short circuit, potentially shutting down the system.

Philips identified that some Allura Xper FD20 Biplane X-ray systems may be missing a drip tray under the cooling unit, either from incomplete past repairs or undocumented installation. Without this tray, coolant liquid could leak onto 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 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.