State
72,992 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Glenview Farms Spreadable Brie is being recalled due to potential Listeria monocytogenes contamination. 754 cases distributed across multiple states are affected.
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Maquet Cardiovascular is recalling the Acrobat SUV Vacuum Stabilizer System (Model C-OM-9000Z) due to manufacturing deviations that compromise the sterile barrier. Sterility cannot be assured during the 2-year shelf life, affecting approximately 10,778 units.
Safecor Health is recalling Docusate Sodium 250 mg softgels due to manufacturing defects where blister card-foils separated from the medication cavity, potentially compromising product integrity.
Lupin Pharmaceuticals is recalling certain lots of Ramipril 5 mg capsules because the active ingredient was sourced from an unapproved vendor, raising concerns about product quality and safety.
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.
EnChroma Inc recalls 53 units of safety glasses with Rx indoor lenses that fail impact safety standards, posing a risk of eye injury. Affected models include Martinez Cx1 Indoor Rx, Summit Indoor Rx, and Martinez Black Cx Rx.
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls.
La Bonne Vie Camembert 8oz cheese (UPC 820581678616, BBD 12/24/2024) is being recalled due to potential Listeria monocytogenes contamination. Approximately 70 cases were distributed across 12 U.S. states.
Safecor Health, LLC is recalling 1,470 boxes of Aspirin 81 mg chewable tablets nationwide due to a manufacturing defect where blister card-foils are separating from the blister cavity.
Olympus is recalling 1,749 GIF-1TH190 gastrointestinal videoscopes to clarify drying procedures in the instructions for use after human errors were identified during evaluation.
Padagis is recalling 10,872 jars of Triamcinolone Acetonide Cream USP 0.025% nationwide because some jars contain subpotent or superpotent active ingredient levels. The defect was discovered during long-term stability testing.
Safecor Health is recalling specific lots of Vitamin D3 25 mcg tablets due to a manufacturing defect where blister card-foils may separate from the blister cavity. No illnesses or injuries have been reported.
Safecor Health recalls 791 boxes of Calcium Carbonate chewable tablets (Lot 24A0073) due to cGMP deviations where blister card-foils separated from blister cavities.
Safecor Health is recalling certain Vitamin B1 supplements due to manufacturing defects where blister card-foils are separating from the blister cavity.
Nestle Health Science is recalling Douglas Labs Stress-B-Plus Dietary Supplement due to incorrect formulation. The product contains Niacin as Nicotinic acid but the label states Niacinamide.
Dr. Reddy's Laboratories is recalling ibuprofen 600 mg tablets for failed tablet specifications. The affected product was distributed nationwide.
GM is recalling certain 2024 Silverado HD and Sierra HD vehicles with power-unlatching tailgates because the gate-release switch may short circuit and unlatch the tailgate.
Maserati is recalling certain 2023-2024 Grecale and 2024 GranTurismo vehicles because park assist module software may prevent the rearview image displaying in reverse.
Volvo Bus is recalling 2025 9700 buses because emergency exit labels may detach, potentially delaying evacuation and increasing injury risk.
Mitsubishi Fuso is recalling 2016-2020 FEC52, FEC72, and FEC92 trucks because the rear leaf spring may break, creating a road hazard.
Winnebago is recalling certain 2024-2025 Ekko motorhomes because the wheel bolts for the spare tire may be missing. 632 units are affected.
Braun Corporation is recalling certain 2024 Chrysler Pacifica and Voyager vehicles because the seat limiter may not have been installed, allowing the seat to move too far forward.
Porsche is recalling 2024-2025 Macan Electric vehicles because the headlights may be too bright, potentially blinding oncoming drivers and increasing crash risk.