State
20,190 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee 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 Tennessee 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.
Sun Pharmaceutical is recalling Amphotericin B for Injection (50 mg vials) due to out-of-specification assay results. The recall affects 11,016 vials with lot numbers BAE0055A, BAE0056A, and BAE0068A distributed nationwide.
Baxter Healthcare is recalling one Spectrum IQ Infusion Pump that underwent improper testing before release. The device was distributed nationwide including in Massachusetts.
Breckenridge Pharmaceutical recalls Duloxetine 20 mg capsules nationwide after detecting N-nitroso-duloxetine impurity above FDA-recommended limits in approximately 7,188 units from lot 220456, expiring February 2025.
NRT X-RAY A/S recalls Intelli-C X-ray tabletops due to faulty firmware and worn motor components that may cause uncontrolled C-arm motion, potentially striking patients or operators.
Philips 5000 Compact Series ultrasound systems may leave unselected transesophageal transducers powered without temperature monitoring, risking patient burns during imaging procedures.
GE Healthcare is recalling certain x-ray systems because adhesive material may not be properly attached to bolts, which could cause components to fall during use.
GE Healthcare recalled certain Allia IGS and related fluoroscopic x-ray systems due to potential incomplete adhesive on bolts in the gantry assembly, risking detector or tube failure.
Randox Laboratories has recalled Clinical Chemistry Calibration Serum (Cal2351/Cal10388) due to negative bias in inorganic phosphate measurements on RX Series instruments. The issue could affect the accuracy of clinical chemistry test results.
Stryker shipped 63 units of cranial mesh labeled as catalog 56-90614 (Gold) but actually containing 56-90314 (Blue) mesh. The mislabeling may cause procedural delays.
Randox Laboratories is recalling 40 units of the Evidence MultiSTAT analyzer because a foam gasket defect may allow light to leak into the camera during testing, potentially affecting result accuracy and delaying reporting.
Acella Pharmaceuticals recalled 7,104 bottles of Sodium Sulfacetamide 10% Sulfur 5% Cleanser nationwide because the product contained less active ingredient than labeled. The recall was terminated in December 2025.
Aurobindo Pharma USA Inc. is recalling 6909 bottles of Clorazepate Dipotassium 7.5 mg tablets due to visible discoloration with yellow and dotted spots. No illnesses or injuries have been reported.
Aurobindo Pharma USA Inc. is recalling Clorazepate Dipotassium Tablets 3.75 mg due to yellow dots and discoloration on some tablets distributed nationwide.
Indian is recalling 2022 Chief and related motorcycles because the kickstand may not properly retract while riding. A failure to retract increases the risk of a crash.
Volkswagen is recalling certain 2023 ID.4 rear-wheel drive vehicles because the 12-volt battery charging cable may wear and cause a short circuit, risking vehicle fire and power loss. Dealers will inspect and repair or replace the cable at no charge.
Bombardier Recreational Products is recalling 2023 Can-Am Spyder F3 and F3-S motorcycles because the rearview mirror lens may dislodge from the housing, reducing driver visibility and increasing crash risk. Dealers will install new mirror assemblies free of charge.
Toyota is recalling 2025 Lexus NX vehicles with loose brake caliper and wheel bearing bolts that may cause brake fluid leaks or wheel detachment. Either condition increases the risk of a crash.
BMW is recalling certain 2025 X3 vehicles due to a potential defect in the front suspension bearing. The bearing may crack, causing loss of vehicle handling and control, increasing crash risk.
Tesla is recalling 2024 Cybertruck vehicles due to a drive inverter fault that may cause loss of propulsion. Affected owners will receive a free inverter replacement.
Lucid is recalling 2024-2025 Air models due to a rear subframe wiring harness that may be too short, causing power loss to the rear drive unit and increasing crash risk. Replacement is free.
Airstream is recalling certain 2019-2024 motorhomes because their tire labels show incorrect pressure and size information. This can lead to under-inflated or incorrectly sized tires, increasing the risk of crashes.
Winnebago is recalling certain 2021-2022 Minnie and Voyage travel trailers due to incorrect cargo carrying capacity labels, which could lead to vehicle overloading and loss of control.
Forest River is recalling 2022-2024 Forester and Sunseeker motorhomes because the park brake signal wire may not be connected to the battery control center, allowing the slideroom to unexpectedly extend during transit and increase crash risk.
Holiday House is recalling 2021–2022 travel trailers because the quick disconnect fittings in the LP gas system may be cracked, causing gas leaks that could lead to fires. Owners should contact Holiday House for inspection and free replacement.
Nova Bus is recalling certain 2010-2024 LFS buses because the driver's seat belt may not retract properly. This can result in a loose seat belt, increasing the risk of injury in a crash.