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All product recalls affecting Delaware.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Delaware in the distribution area.
General Motors, LLC (GM) is recalling certain 2020-2022 Chevrolet Bolt EV and 2022 Chevrolet Bolt EUV vehicles that were previously remedied under recall number 21V-650. The advanced diagnostic software may have been incorrectly installed and fail to detect defective battery modules, possibly resulting in a battery fire.
If temperature management system fails to reach correct target water temperature while device is operating in patient control mode, due to sudden patient temperature changes/interruption in water flow/blockage of air flow by an obstruction or dirty filter, then system may not alert, and alarm absence may lead to hypothermia or hyperthermia, so a software update will be released to correct issue.
The recalled Hayden bookcase contains six storage cubbies, and is made of brown wood with three sliding white doors. It measures 35.5 inches in width, 16 inches in depth, and 73 inches in height. A label located on the back of each unit contains the product name and SKU number LB2225/A.
This recall involves Brookstone TurboVac Handheld Rechargeable Vacuums (Model No. BSBVAC301). The model number is printed on the back of the unit. "Brookstone" is printed on the top front of the vacuum. The vacuums are black and come with a wall-plate for hanging on the wall, and they measure 2.89 x 12 inches in dimension.
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024 Lexus RX 350, RX 350h, 2024-2025 NX 250, NX 350, and NX 350h vehicles. The head restraints on the driver and front passenger seats may be inadvertently removed without pressing the lock release button. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) Number 202, "Head Restraints."
Power Stop LLC (PowerStop) is recalling certain Braided Steel Brake Hoses. Please see the attached document for a complete list of part numbers. The brake hoses may leak and also may be labeled incorrectly. As such, these brake hoses fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 106, "Brake Hoses."
The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
This recall involves REI Co-op Cycles REV 12-, 16-, or 20-inch kid's bicycles (all model years 2022-2024). Serial numbers included in the recall begin with "ET22," "ET23," "01VX" or "07VX." The serial number is printed underneath the bike frame on the bottom bracket or down tube. Brand Model SKU/Article # Color Co-op Cycles REV 12 Kids Bike 190741 BONDI (green) Co-op Cycles REV 12 Kids Bike 190741 PENCIL (yellow) Co-op Cycles REV 16 Kids Bike 190742 SURFS UP (blue) Co-op Cycles REV 16 Kids Bike 190742 CATCH UP (red) Co-op Cycles REV 16 Kids Bike 190743 FOUR LEAF (green) Co-op Cycles REV 20 Kids Bike 190743 PLUM BURST (purple)
Altec Industries, Inc. (Altec) is recalling certain 2021-2024 JEMS S and JEMS SE vehicles. Inadequate clearance between the A/C hoses and the engine exhaust manifold may result in the hoses overheating.
This recall involves Baseus power banks with model numbers PPCXM06 and PPCXW06. Both PPCXM06 and PPCXW06 were offered in white, black, light blue, and light pink colors. Both models have a magnetic side that attaches to mobile phones with magnetic charging functionality. The model number is displayed on the magnetic side of the device, and "20W" is displayed on the non-magnetic side. Model PPCXM06 measures about 4 in. x 2-½ in. x 0.64 in., and model PPCXW06 measures about 4 in. x 2-½ in. x ½ in. Only power banks with model numbers PPCXM06 and PPCXW06 are part of this recall. Some power banks were listed on Amazon under the model number PPXCW06.
This recall involves Tie Dye Fur Toy Trunk Storage Chests, sold in two sizes. The large chest has dimensions of about 32-½" x 16-½" x 21". The small chest has dimensions of about 27" x 13-½" x 16-½". The chest is made of MDF wood board, and is covered in a multi-color tie dye patterned faux fur fabric.
This recall involves Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps that provide heating and cooling. The recalled units are beige and the model name is printed on the outside of the unit. The model number is located on the serial plate on the side of the unit. The following model numbers are included in this recall: Recalled Daikin FIT Recalled Amana S-Series Recalled Goodman SD DZ6VSA1810-AA ASZS601810-AA GSZS601810-AB DZ6VSA1810-AB ASZS601810-AB GSZS602410-AB DZ6VSA2410-AA ASZS602410-AA GSZS603010-AB DZ6VSA2410-AB ASZS602410-AB GSZS603610-AB DZ6VSA241E-AB ASZS60241E-AB DZ6VSA3010-AA ASZS603010-AA DZ6VSA3010-AB ASZS603010-AB DZ6VSA3610-AA ASZS603610-AA DZ6VSA3610-AB ASZS603610-AB
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2008-2024 G5, 2008-2015 MBII, and 2015-2023 T-Series transit buses. The rear emergency door exterior handle may unexpectedly break under applied force.
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.
Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
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Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.