State
73,100 recalls have nationwide distribution and so reach West Virginia. 3,570 additional recalls listed West Virginia specifically in their distribution scope.
Of the 3,570 recalls naming West Virginia we have scored against our rubric, 603 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 669 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,570 recalls whose distribution notice names West Virginia specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2023-2024 Aerial Device, Digger Derrick, and Pressure Digger vehicles due to an overloaded chassis ignition circuit that can cause engine shutdown and increase crash risk.
The rearview camera image may not display on certain 2024 Land Rover vehicles due to a faulty Near Field Sensing Module that can overheat. Dealers will replace the module at no cost.
General Motors is recalling certain 2023-2024 trucks and SUVs because the brake fluid warning light may fail to display, potentially causing unsafe driving conditions with low brake fluid.
Kawasaki is recalling 2024 Z7 Hybrid and Ninja 7 Hybrid motorcycles because the electronic control unit may cause the transmission to shift into neutral, increasing crash risk.
General Motors is recalling certain 2024 GMC Canyon vehicles because the headlights may flicker while driving or parked, reducing visibility and increasing crash risk. Dealers will replace the headlight module at no cost.
JFE FRANCHISING INC is recalling Pico de Gallo Classic products in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should return them to the place of purchase or discard them.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for the Trilogy Evo Universal Ventilator to address safety issues identified in earlier recalls. Affected units should implement the update.
Baxter Healthcare Corporation is recalling 44,208 containers of Heparin Sodium in Sodium Chloride Injection nationwide after endotoxin testing revealed out-of-limit results. The contamination poses a risk of serious adverse reactions in patients receiving the intravenous medication.
JFE Franchising is recalling medium and mild salsa products sold in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination.
JFE Franchising is recalling guacamole products due to Listeria monocytogenes contamination. Affected items were distributed in Kentucky, Michigan, Ohio, and West Virginia with sell-by dates from July 9 to July 26, 2024.
Storyteller Overland is recalling 2024 GXV Hilt vehicles because the spare tire mount may not be secured properly, allowing the tire to detach.
Tiffin is recalling 2022–2025 Allegro Bay motorhomes due to subframe truss collapse that can pinch electrical wiring and cause electrical arcing, increasing fire risk.
Trail King is recalling 2019-2020 TKHDG Paver Special trailers because the gooseneck lift lower cylinder mount may crack, causing the trailer to drop suddenly.
JFE Franchising Inc recalls 5oz packages of chopped cilantro with white onion due to potential Listeria monocytogenes contamination. Affected products were distributed in Kentucky, Michigan, Ohio, and West Virginia.
Butternut squash cubes sold in Kentucky, Michigan, Ohio, and West Virginia are recalled due to potential Listeria monocytogenes contamination. Affected products have sell-by dates between July 9 and July 26, 2024.
Unilever North America is recalling Popsicle Jolly Rancher Frozen Confection Pops nationwide due to undeclared milk, which poses a risk to consumers with milk allergies.
Breas Medical is recalling the Vivo 45 LS ventilator due to potential elevated formaldehyde emissions into the patient breathing airpath under specific conditions.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo EV300 ventilators to resolve previously identified safety issues. Approximately 90,910 US units and 56,273 international units are affected.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo ventilators worldwide to resolve identified safety issues. Users must apply the update and review the updated User Manual.
JFE FRANCHISING INC is recalling diced pepper and fajita mix products sold in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination. Consumers should discard the products or return them to the store.
The BD Pyxis QFill Replenishment Station medication cabinet has a software issue that may print incorrect bin information on restock labels for medications stored in non-CUBIE locations.
Abiomed is updating labeling for the Impella CP Smart Assist Set to warn about a potential interaction with the Shockwave Coronary IVL Catheter when used during coronary interventions. The interaction was previously undocumented in the device instructions.
The adhesive joint in this medical device component can fail, causing the metal part to detach. This may damage the centrifuge, destroy patient samples, and potentially expose lab staff to biohazardous material.
ProRx LLC is recalling 37 vials of compounded Tirzepatide injectable due to lack of sterility assurance. The 2 mL vials (10 mg/mL and 20 mg/mL) were distributed nationwide.
ProRx LLC is recalling Tirzepatide 20 mg/2mL injectable vials nationwide due to lack of assurance of sterility. Patients who received vials from lot ProRx051424 should contact their healthcare provider.