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All product recalls affecting Kansas.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Kansas in the distribution area.
Two new potential laser safety failure modes have been identified in the product design. Overcurrent of laser diode, and a fail-unsafe mode. The failure modes have never been found to occur in these models, whether in the field or factory, but could potentially occur under excessive force or extreme, continuous vibration.
Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage.
Potential for open header bag seals, compromising sterility.
The Heil Co. (Heil) is recalling certain 2020-2023 Side Loader garbage trucks. The battery support bracket may break and damage the battery case, possibly resulting in a battery rupture.
Winnebago Industries, Inc. (Winnebago) is recalling certain 2024-2025 Ekko recreational vehicles. The inner wheel tire valve extension may be damaged through contact with the outer wheels, causing the inner tire to lose air pressure and overload the outer tire.
Lack of Assurance of Sterility.
Potential for open header bag seals, compromising sterility.
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Lack of Assurance of Sterility.
Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.
Bendix Commercial Vehicle Systems, LLC (Bendix) is recalling certain Knorr-Bresme 22/24-57 brake chambers, with part number K068622 and K038830N00, sold as replacement parts for certain buses. The brake chamber may have been improperly manufactured, which can result in an air leak.
Potential that a component (air baffle) may be missing in some Nehalem FlexVision-2 PCs that are part of the Allura Xper series.
Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.
This recall involves Amazon Basics Premium Foam Eurotop Mattresses. The mattresses are nine inches thick and were sold in twin, full, queen and king sizes. They have a white top panel and a gray side panel with an Amazon Basics tag on the foot panel. They were manufactured from December 22, 2022, through May 16, 2024. The manufacture date in MM/DD/YYYY format; SKU number ABFM0933, ABFM0946, ABFM0950 or ABFM0966; and prototype ID: 1131 40 00 1 appear on a white label located on the center seam of the foot panel.
This recall involves four different styles of Baby Loren Morning children's 100% cotton loungewear dresses. The loungewear was sold in floral tulips, princess and castle and unicorn and butterfly prints and in sizes 2T, 3T, 4T, 5Y and 6Y. The Baby Loren logo, the size, "October 2022" or "October 2023" and a batch number ending in 3465, 3585, 3599 or 3569 are printed on sewn-in neck labels.
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.