State
73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2023-2024 BrightDrop Zevo 600 vehicles with optional passenger jump seats due to a trim panel that may interfere with the right-side roof-rail air bag.
Hyundai Translead is recalling 2022-2024 extended chassis because improperly welded cross braces may detach, posing a road hazard or causing brake lock.
T.A. Pelsue is recalling 2022 Fiberlite POD and XL Tradesman trailers because the welded tongue may detach, increasing crash risk.
Family Health Products is recalling Crystal Clear Sodium Hydroxide sold on Amazon because the packaging is not child-resistant as required by law. The product poses a risk of chemical burns and eye irritation if accessed by children.
Gevi countertop nugget ice makers with model number GIMN-1102 and a date code before June 1, 2022, are being recalled because metal auger blades can break and create sharp metal pieces in the ice basket, posing a laceration risk. No injuries have been reported.
General Motors is recalling certain 2023 Cadillac Lyriq vehicles due to a software defect in the body control module. The pedestrian warning sounds may fail to activate, creating a crash risk.
YourHealthToolkit is recalling about 280 children's 5-pound weighted blankets sold on Amazon.com from January through March 2020. A young child can become entrapped inside the blanket by unzipping it, posing a risk of death by asphyxiation.
Southeast Toyota Distributors is recalling certain 2023 Toyota 4Runner vehicles due to an incorrect load carrying capacity modification label. The error could result in vehicle overloading and increased crash risk.
About 13,250 FORT children's play tents are being recalled because magnets used to connect pieces can come loose, posing choking and laceration risks to young children. The manufacturer is no longer in business and offers no remedy.
General Motors is recalling 2023 GMC Acadia vehicles and certain 2024 Cadillac models due to windshields that may not be properly bonded to the vehicle body. A detached windshield during a crash could increase the risk of injury.
Little Sleepies is recalling approximately 450,000 Sleepyhead Loveys and Bandana Bibs because the care instruction label can detach, posing a choking hazard to young children.
Dr. Berne's MSM DROPS 5% Solution was recalled by the FDA for non-sterility issues. Lot 6786, with expiration date March 31, 2025, is distributed nationwide and internationally.
Allison Transmission is recalling specific B3400 and B400R models because the transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.
Certain lots of Guider Softip Guide Catheters were manufactured with an incorrect tip curve shape that differs from labeled specifications. The recalled devices include 17,436 units distributed in Indiana.
Boston Scientific is recalling Guider Softip Guide Catheters (Catalog M003101440) in certain lots due to incorrect tip curve shape that differs from the labeled specification. The recall affects 2,184 units.
Central Admixture Pharmacy Services Inc is recalling phenylephrine injectable syringes nationwide due to lack of assurance of sterility. The recall affects 19,510 units distributed across multiple lot numbers.
AB Sciex is recalling 14 Citrine Triple Quad Mass Spectrometers (Part Number 5063684) due to rare risk of solvent leak and electrical discharge potentially causing flame and electrode ejection at the ion source probe.
Central Admixture Pharmacy Services is recalling lidocaine 2% injectables due to inability to assure sterility. Approximately 1,992 syringes distributed nationwide are affected.
Central Admixture Pharmacy Services is recalling midazolam injectable solution syringes due to lack of assurance of sterility. Patients should not use the affected lots and consult their healthcare provider.
Central Admixture Pharmacy Services Inc. is recalling fentanyl injectable solution nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.
Icecure Medical Ltd is updating the user manual for IceCure Cryoablation System ProSense surgical devices to add safety guidelines for managing mechanical damage such as bent cryoprobes.
Guider Softip XF Guide Catheters were distributed with an incorrect tip curve shape differing from labeled specifications, affecting 1,086 units in Indiana.
Central Admixture Pharmacy Services is recalling 598 fentanyl syringes due to lack of assurance of sterility. The affected lots were distributed nationwide.
Boston Scientific is recalling certain lots of Guider Softip Guide Catheters due to an incorrect tip curve shape. The affected devices were distributed with a different tip curve than labeled.
Central Admixture Pharmacy Services Inc. is recalling hydromorphone syringes due to lack of assurance of sterility. The recall affects 274 syringes distributed nationwide.