State
20,324 recalls have nationwide distribution and so reach Alabama. 0 additional recalls listed Alabama 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 Alabama 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.
Canon Medical has recalled 12 INFX-8000C tableside consoles due to a printed circuit board that may require replacement. Though procedures may be delayed, x-ray operations can continue using alternative controls.
BMW recalls certain 2022-2023 iX, i4, and 2023 i7 models due to a high voltage battery ECU software issue that may interrupt electrical power and suddenly disable drive power.
Harley-Davidson is recalling certain 2023 FLHXSE motorcycles due to an engine control module software defect that may cause loss of control at high speeds, increasing crash risk.
Sensio Inc. is recalling approximately 860,000 electric and stovetop pressure cookers because the lid can unlock and be removed during use, causing hot contents to splash out and burn consumers. The company has received 63 incident reports, including 61 burn injuries with some involving second and third degree burns.
Polaris recalls about 27,300 Model Year 2021 RZR XP Turbo and RZR Turbo S recreational off-road vehicles because the clutch can fracture and eject fragments, causing fires and injuries. Owners should stop using the vehicles and contact Polaris for a free clutch replacement.
Ford is recalling certain 2023 E-450 vehicles because rear axle rotor bolts may be improperly tightened, risking wheel separation and increasing crash risk. Dealers will replace affected assemblies at no charge.
The Children's Place is recalling about 97,400 units of Baby and Toddler Boy Basic Stretch Straight Leg Jeans because metal snaps can detach, posing a choking hazard to young children. No injuries have been reported.
Restwell Mattress Co. is recalling about 100 Room & Board brand crib mattresses because they fail to meet federal safety standards and pose a suffocation hazard to infants. Consumers should stop using the mattresses and contact Room & Board for a refund.
13131 Imports is recalling Red Apple Fireworks brand "American Glory" and "Merica AF" shell fireworks due to risk of premature explosion and burn injuries. The firm has received 72 reports of premature explosions, though no injuries have been reported.
Polaris Industries is recalling about 12,300 off-road vehicles and fuel system parts because a fuel leak can occur at the fuel pump outlet connector near a hot surface, posing a fire hazard. No fires or injuries have been reported to date.
Ford is recalling certain 2022 Bronco Sport vehicles due to a fuel pump control module bracket that may not be properly secured to the fuel tank. If the bracket fails, the engine may stall, increasing the risk of a crash.
Target is recalling about 2.2 million Threshold Glass Jar Candles because the glass jars can crack or break during use, posing laceration and burn hazards. Target received 19 reports of jars breaking or cracking, resulting in one minor injury.
Saxco International is recalling about 8,370 glass carboys because the glass can break due to improper cooling processes, posing a laceration hazard. The firm has received 30 reports of incidents of glass breaking, though no injuries have been reported.
Lupin Pharmaceuticals is recalling TYDEMY birth control tablets due to failed stability testing. Consumers should contact their healthcare provider.
The Impella RP Flex cardiac pump has been recalled due to a higher-than-expected rate of blood clot formation. Blood clots may reduce cardiac support or cause hemolysis.
Ford is recalling 2020-2022 Lincoln Aviators and Ford Explorers with 3.0L plug-in hybrid engines. A high-voltage battery manufacturing defect may cause battery failure, loss of drive power, and fire risk.
Ford is recalling 2025 E-350 trucks and related models due to a transmission park pawl casting defect that may not fully engage, potentially causing vehicle rollaway.
Central Admixture Pharmacy Services recalls 128 neonatal TPN starter bags distributed nationwide due to lacking validation of decontamination procedures, creating inability to assure product sterility.
Central Admixture Pharmacy Services is recalling cardioplegia solution IV bags nationwide due to lack of validated sterilization processes. The recall affects 184 bags from two lots.
Central Admixture Pharmacy Services is recalling 1,927 bags of vancomycin IV bags (750 mg/250 mL) distributed nationwide due to lack of sterility assurance and insufficient decontamination validation.
Olympus is recalling endobronchial navigation needles because an electromagnetic sensor malfunction can disable navigation guidance during medical procedures, potentially causing procedural delays.
Central Admixture Pharmacy Services has recalled Cardioplegia Solution due to lacking sterility assurance and insufficient validation data for decontamination cycles. The recall affects 148 bags distributed nationwide.
Medline recalls 4,618 custom sterile procedural kits distributed worldwide from April 2020 through April 2023. The Turkuaz ultrasound gel component may not meet sterility specifications, posing a potential infection risk in surgical procedures.
Central Admixture Pharmacy Services is recalling 12 IV bags of Transplant Solution nationwide (Lot 36-252141) because the sterilization decontamination cycles lack proper validation, creating a sterility assurance deficiency.
Medline Industries is recalling 148,445 procedural kits containing Turkuaz Ultrasound Gel over potential sterility failure of the gel component, which could lead to infections if used in sterile procedures.