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.
Central Admixture Pharmacy Services recalls 150 fentanyl injection syringes nationwide because sterilization procedures were not properly validated.
Central Admixture Pharmacy Services is recalling 6,782 bags of vancomycin IV bags distributed nationwide due to lack of validation data for decontamination cycles, which compromises sterility assurance.
Central Admixture Pharmacy Services is recalling 9,121 epinephrine IV bags distributed nationwide due to lack of sterility assurance and insufficient validation data for decontamination cycles.
Vecuronium injection syringes were recalled nationwide due to lack of validation data for sanitization cycles, which raises sterility assurance concerns.
FDA is recalling Central Admixture Pharmacy Services' neostigmine injectable syringes due to lacking validation data for sterilization decontamination cycles, raising concerns about product sterility.
Central Admixture Pharmacy Services Inc. is recalling 16,971 syringes of phenylephrine injection due to lack of validation data for sterilization processes. The product was distributed nationwide.
Medline is recalling custom sterile and non-sterile procedural kits containing Turkuaz Ultrasound Gel due to potential sterility specification failures. The kits were distributed worldwide to hospitals and medical facilities.
Medline is recalling 13,881 sterile procedural kits worldwide due to potential sterility failure in the ultrasound gel component. The affected kits are used in various medical insertion procedures.
Medline Industries recalls 19,907 procedural kits because the sterile ultrasound gel component may not meet sterility specifications.
Central Admixture Pharmacy Services is recalling oxytocin IV bags nationwide due to insufficient validation of sterilization decontamination processes. The recall affects 6,037 bags distributed across multiple lots.
Microtek Medical Inc. is recalling certain lots of surgical table drapes and infection control kits due to detection of naphthalene odor. The affected products are distributed nationwide in the US and in Canada.
The Ritedose Corporation is recalling Cromolyn Sodium Oral Solution (Concentrate) due to a manufacturing deviation. Lot 23CE2, distributed nationwide, was released prior to obtaining required supplier approval.
Creganna Medical Devices is recalling three lots of Gore Tips Set Device due to incorrect expiration date labeling. Affected devices may be used past their actual expiration date.
Microtek Medical Inc. is recalling certain lots of Ecolab sterile medical device drapes due to naphthalene odor. The recall affects five models distributed in the United States and Canada.
Volkswagen is recalling certain 2021-2022 Atlas Cross Sport vehicles due to an infotainment system defect that may prevent the rearview camera image from displaying. This loss of rear visibility increases crash risk.
Alliance RV is recalling 2022-2023 Paradigm and Valor travel trailers due to electric retractable awning weld separation that may allow the awning to drop unexpectedly, increasing injury risk.
Tiffin is recalling certain 2021-2023 Allegro and related motorhomes due to a defective LPG tank connection that may cause propane leaks and fire risk. Free inspection and repair are available through Tiffin dealers.
BMW is recalling 2022 X3 xDrive30i vehicles because the high-pressure fuel rail may crack and cause a fuel leak in the engine compartment, increasing the risk of fire. Dealers will replace the fuel rail free of charge.
Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.
Chrysler is recalling certain 2022-2023 Jeep Grand Cherokee and 2021-2023 Jeep Grand Cherokee L vehicles. Rear coil springs may detach while driving, creating a crash risk; dealers will repair them free.
Certain 2023 Hyundai Palisade vehicles have a brake booster defect that can cause loss of power brake assist, requiring longer stopping distances and increasing crash risk.
Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.
Forest River is recalling 2021-2022 Coachmen motorhomes with defective cooktop burner valves that can develop gas leaks. The leaks pose a fire risk and will be remedied by free cooktop replacement.
Mercedes-Benz USA is recalling certain 2017-2022 models after a communication module software error disabled the emergency eCall system. Owners can receive a free software update via over-the-air delivery or at a dealer.
BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.