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All product recalls affecting West Virginia.
Includes nationwide recalls (tagged “Nationwide”) and recalls with West Virginia in the distribution area.
Oshkosh Corporation (Oshkosh) is recalling certain 2025 Defense NGDV ICE vehicles. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility."
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.
Chrysler (FCA US, LLC) is recalling certain 2024 Jeep Grand Cherokee and Grand Cherokee L vehicles. The radiator crossmember bolts may not be properly secured, which can lead to improper air bag deployments and a fuel leak during a crash. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 208, "Occupant Crash Protection" and 301, "Fuel System Integrity."
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.
Vagus nerve stimulator generators may stop delivering stimulation due to an internal, mechanically activated component that may become stuck in a closed position, which may result in patients returning to baseline seizure frequency or depressive symptoms and in the longer term, patients may be required to undergo generator replacement surgery to replace their device.
Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR) alarm and loss of Central Venous (CV) Placement Signal, Pulmonary Artery (PA) Placement Signal & Pulmonary Artery Pulse Index (PAPi) metrics. Abiomed is reinforcing that there is a risk of potential interaction between the tip of guidewires, indwelling central venous lines or devices and inlet of the Impella pumps listed above during the insertion, manipulation, and removal of those devices. The interaction may result in optical sensor damage, temporary pump stop, or permanent pump stop.
This recall involves all Stanley Switchback and Trigger Action stainless steel travel mugs sold in the United States. The recalled double-walled mugs were sold in a variety of colors including white, black and green, in 12 oz., 16 oz. and 20 oz. sizes with a polypropylene lid. The Stanley logo appears on the front and bottom of the mug. The recalled mugs have one of the following product identification numbers printed on the bottom of the mug. Name Size Product Identification Number Switchback 12 ounces 20-01437 16 ounces 20-01436, 20-02211 Trigger Action 12 ounces 20-02033, 20-02779, 20-02825 16 ounces 20-02030, 20-02745, 20-02957 20 ounces 20-02034, 20-02746
This recall involves the Yoto Mini, a portable connected screen-free speaker intended for children ages three to twelve. The Yoto Mini is operated by use of Yoto cards and is designed to play audiobooks, music, radio and podcasts. The speakers are pale gray with orange tactile controls and a pixel display. The model name Yoto Mini, SKU PRPLXX00860, and serial number are located on the base of the product. The recalled Yoto Mini was sold with a charging cable included but no adaptor or charger.
This recall involves the Wall Teester Bed Crowns. The product is a decorative crown mounted on the wall over a bed with mounting brackets that screw to the wall. The welded tabs attach to the teester. The bed crowns were sold in the following styles, colors, SKU number and measurements. The model number is printed on a label on the outside of box. Style and Color Model SKU Number Measurements Valensia Wall Teester Bed Crown Platinum AW42 29 inches x 8.5 inches x 10.5 inches Victoriana Wall Teester Bed Crown Natural Cherry AT36 29 inches x 8.5 inches x 10.5 inches Viviana Wall Teester Bed Crown Antique Ivory AT37 29 inches x 8.5 inches x 10.5 inches Valeria Wall Teester Bed Crown Aged Gold AW41 29 inches x 8.5 inches x10.5 inches Victoria Rose Wall Teester Bed Crown Antique Ivory and Stain Gold AW43 24 inches x 9.5 inches x 9.5 inches
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
General Motors LLC (GM) is recalling certain 2025 Chevrolet Equinox EV vehicles. The pedestrian alert sound system may have incorrect software and not produce sound at a sufficient volume. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 141, "Minimum Sound Requirements for Hybrid and Electric Vehicles."
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit