State
72,968 recalls have nationwide distribution and so reach West Virginia. 3,541 additional recalls listed West Virginia specifically in their distribution scope.
Of the 3,541 recalls naming West Virginia we have scored against our rubric, 593 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 657 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jaguar is recalling certain 2021-2024 E-Pace vehicles because the passenger air bag may tear during deployment. 1,436 vehicles are affected.
Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.
Unbranded braided crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct breathing. About 260 units are affected.
Creekliybear "Pack and Play" aftermarket play yard mattresses are being recalled because they exceed thickness requirements and may not fit certain play yards. About 21,500 units affected.
AUGNORYE padded cushioned crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct an infant's breathing. About 356 units are affected.
Dearlomum retractable mesh safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor. About 2,200 units are affected.
SPPTTY kids 14- and 18-inch bicycles are being recalled because multiple components contain lead exceeding the federal lead content ban. About 200 units are affected.
WLIVE Fabric 15-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the federal standard under the STURDY Act. About 6,600 units affected.
Momentum Vida E+ e-bikes are being recalled because the fork steerer tube can crack, break or separate during use, posing a fall hazard. About 6,200 units are affected.
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Philips Respironics is recalling BiPAP A30 and BiPAP Hybrid A30 ventilators. The devices do not have an indication for use in patients with respiratory failure.
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.