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.
Glenmark Pharmaceuticals is recalling Fluocinolone Acetonide Oil 0.01% ear drops due to failed excipient specifications. The affected lots nationwide do not meet required quality standards for isopropyl alcohol content.
Sun Pharmaceutical is recalling 11,400 bottles of Lurasidone Hydrochloride 60mg tablets due to microbial contamination in manufacturing equipment. Patients taking this medication should contact their doctor or pharmacist.
Achieva 1.5T MR systems have incorrect warning labels on the Liquid Cooling Cabinet, missing the high voltage warning symbol. This presents a potential electrical shock risk for service personnel.
Sun Pharmaceutical recalls 55,272 bottles of Febuxostat 40mg tablets nationwide due to microbial contamination detected in manufacturing equipment. No illnesses have been reported.
Some Philips Intera 1.5T MRI systems have an incorrect warning label on the Liquid Cooling Cabinet that fails to properly warn service personnel of electrical shock hazards.
Pacific Cycle is recalling about 1,700 Ascend Cabrillo and Minaret electric bikes because the battery charging wiring harness may overheat and catch fire while charging. The company has received three fire reports, including one causing second-degree burns.
Clark Associates is recalling about 53,800 Allegro plastic side chairs because the chairs can break apart while in use, creating a fall hazard. The company has received 16 reports of chairs breaking apart, resulting in two injuries.
About 12,440 Yaomiao children's tiaras with rhinestones sold on Amazon.com contain lead levels that exceed federal limits. Lead is toxic if ingested by young children and can cause adverse health effects.
BRS Fuel Bottles sold on Amazon from December 2020 through October 2023 do not have child-resistant closures as required by law, posing a risk of burn and poisoning to children. Consumers should stop using them immediately and contact the distributor for return or disposal.
Visual Comfort & Co. is recalling Maverick Coastal 60-inch outdoor ceiling fans because the blades can crack or break and fall, posing an impact injury hazard. The manufacturer has received nine reports of blade failure but no injuries or property damage so far.
Maquet Cardiovascular is recalling Express chest drain units with defective sterile water syringes. If not kept upright, patients risk exposure to infectious material that may cause infection, abscess, sepsis, or death.
The FDA has recalled Secret Dry Spray Antiperspirant due to benzene contamination in certain lots. Affected products were distributed nationwide in the USA, Puerto Rico, Canada, and internationally.
Pfizer is recalling 34,000 cartons of 4.2% Sodium Bicarbonate Injection nationwide due to glass particles in the solution. Patients should immediately stop use and contact their supplier.
Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to benzene contamination in specific lot numbers. The FDA has classified this as a Class I recall.
Pfizer Inc. is recalling 21,200 cartons of Sodium Bicarbonate Injection (lot HA7295, expiring March 1, 2025) nationwide due to glass particle contamination. The product is distributed in the United States and Puerto Rico.
Americaine benzocaine 20% topical anesthetic spray is being recalled nationwide due to benzene chemical contamination. The recall affects 34,704 cans with lot number 1A16420 and expiration date 01/31/2025.
Old Spice Sweat Defense Ultimate Captain anti-perspirant spray is being recalled due to benzene contamination. The FDA Class I recall affects products distributed nationwide and internationally.
Old Spice PURE SPORT Anti-Perspirant Spray is recalled for benzene contamination in certain lot numbers. The product was distributed nationwide and internationally.
Mead Johnson is recalling Enfamil Nutramigen Hypoallergenic Infant Formula Powder due to potential Cronobacter sakazakii contamination. Approximately 1.4 million cans with specific UPC codes (300871239418 or 300871239456) and January 1, 2025 use-by date are affected.
The FDA is recalling Secret Dry Spray antiperspirant (Lot #12001458SF) due to benzene contamination. Consumers should stop using the product immediately.
Pfizer Inc. is recalling Atropine Sulfate Injection due to glass particulate matter contamination in lot GY2496. This FDA Class I recall affects 24,400 cartons distributed nationwide in the USA and Puerto Rico.
Old Spice Sweat Defense Pure Sport Plus anti-perspirant spray is being recalled nationwide due to benzene contamination in specific lot numbers. Consumers should discontinue use of affected products immediately.
Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.
The Procter & Gamble Company is recalling Secret antiperspirant/deodorant spray due to the presence of benzene, a chemical contaminant. The recall affects multiple lot numbers distributed nationwide and internationally.
A surgical guide used in knee replacement is recalled due to mislabeling showing incorrect dimensions. This could result in improper bone resection and implant fit, potentially extending surgery time.