State
20,199 recalls have nationwide distribution and so reach Arkansas. 0 additional recalls listed Arkansas specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Arkansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
The CPSC has recalled about 2,000 Vibe Bear playyard mattresses sold on Amazon.com from January to June 2023 due to suffocation hazard to infants. The mattresses violate federal crib mattress safety regulations and lack required warnings and labels.
Security Equipment Corporation is recalling about 4,000 SABRE Aim & Fire Pepper Gel Spray canisters with expiration date 9/2027 because they lack a red nozzle needed to deploy the spray and will not function in an emergency. No injuries have been reported.
Wet & Forget USA is recalling about 2.7 million bottles of "Xtreme Reach" Outdoor Mold & Mildew Stain Remover with hose end nozzles. The nozzle clip can dislodge, spraying cleaning solution on users and causing skin and eye irritation.
Mary Meyer is recalling about 1,950 Bubba Bull Plush Toys because the eyes can break off and pose a choking hazard to young children. No injuries have been reported.
SourceOne Ventures recalls Windsor Queen Xtrabed Mobile Murphy Beds due to risks of cabinet breakage and tip-over. About 12,000 units sold at Wayfair between November 2016 and April 2023 are affected.
Polestar is recalling certain 2023 Polestar 2 vehicles due to a defect in the front left lower ball joint that could cause loss of steering control. Owners should contact their dealer for a free inspection and replacement.
Moonsea Pack and Play Mattresses sold on Amazon violate federal crib mattress safety regulations and pose a suffocation hazard to infants. Consumers should stop using them immediately and contact Moonseasleep for a refund.
Nova Bus is recalling certain 2019-2023 LFS and LFS Artic transit buses. The transmission yoke may separate, causing driveshaft separation and sudden loss of drive power, increasing the risk of crashes and passenger injury.
Bugaboo is recalling about 1,000 Dragonfly Seat Strollers because the backrest can move downward in parent-facing mode, causing unrestrained infants to potentially tumble from the seat. No U.S. injuries have been reported.
The electric cord plug prong on Oreck Discover Upright Vacuums can detach and remain in electrical outlets, creating an electrical shock hazard. About 6,200 units sold nationwide from September 2022 through September 2023 are affected.
Bunkhouse and Lotsa LITES! Connectable Mini String Lights can overheat and present burn and fire hazards when plugged directly into an outlet. About 34,600 units are affected.
Ergodyne is recalling about 16,570 Squids 3705 Wire Tool Attachments because the wire can break when dropped while tethering a tool over two pounds, posing an injury risk to bystanders below.
Botanical Be is recalling 235 bottles of Artri King tablets sold nationwide. The tablets contain undeclared diclofenac and were marketed without FDA drug approval.
Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.
The 2022 Nissan Sentra may have a defective driver's side cowl seal, allowing water intrusion and electrical corrosion. This could cause loss of airbag function, exterior lighting, and braking safety features, increasing crash and fire risk.
Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.
Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.
Apotex Corp. is recalling Paroxetine Hydrochloride 40 mg tablets nationwide due to failed quality specifications. Testing found out-of-specification impurity levels in affected lot numbers.
Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.
Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.
Certain 2020-2022 Nissan Frontier and Titan vehicles have a defective transmission parking pawl that may not engage when shifted to park, creating a rollaway risk. Dealers will replace the component at no cost.
Apotex Corp. is recalling nationwide 25,776 units of Paroxetine Hydrochloride 30 mg tablets due to out-of-specification impurities. Affected lot numbers RV8686, RX0119, and RV2254 expire 08/2024.
Breas Medical is recalling 215 mouthpiece units due to manufacturing defects with unintended slits that may result in insufficient ventilation in mechanical ventilation patients.
Paroxetine tablets are being recalled for failing specification tests due to higher-than-acceptable levels of a degradation impurity. Approximately 1,941 bottles distributed nationwide are affected.
Forest River is recalling 205 2022 R-POD travel trailers because the Federal Placard shows an incorrect axle rating (4400 lbs instead of 3500 lbs), which can cause overload and loss of control.