State
73,478 recalls have nationwide distribution and so reach Indiana. 9,589 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,589 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,589 recalls whose distribution notice names Indiana specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Crate and Barrel is recalling about 620 Be the Band Music Sets because the maracas can break or become unscrewed and release metal beads that pose choking and suffocation hazards to young children.
Microbiologics Inc is recalling Helix Elite Molecular Standards for Inactivated Influenza A/B and Respiratory Syncytial Virus because shelf life testing failed at 24 months, potentially affecting product stability.
Lacrimedics is recalling Collagen Plugs (models CP3, CP4, CP5) due to potential seal integrity defects in sterile pouches. The seals may contain channels that could compromise sterility and allow contamination.
Microbiologics has recalled KWIK-STIK quality control kits due to a specific lot failing to meet resistance specifications for Gentamicin Synergy. The affected bacterial strain showed unexpected susceptibility when it should have been resistant.
Beckman Coulter is recalling 181,776 AU/DxC AU Magnesium test kits because the test may give falsely elevated results in lipemic samples, potentially affecting clinical interpretation.
A quality control negative control material in GBS diagnostic testing sets is yielding false-positive results, causing laboratory test failures and operational disruptions.
TSM Brands LLC is recalling Luxury 70% Isopropyl Alcohol bottles nationwide because the product contains undeclared ethyl alcohol that is not identified on the label.
TSM Brands LLC is recalling 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen due to undeclared ethyl alcohol in the product. The recall affects bottles distributed nationwide.
Microbiologics Inc is recalling its Helix Elite Extended Enteric Bacterial Verification Panel because real-time shelf life testing failed at 24 months.
Macleods Pharma USA is recalling one lot of Amlodipine and Olmesartan Medoxomil Tablets nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and was initiated by the manufacturer.
Microbiologics QC sets used for GBS testing contain a negative control contaminated with Group B Streptococcus, causing test failures. Affects 541 units distributed nationwide.
Preferred Pharmaceuticals is recalling 276 bottles of Alprazolam Tablets USP 1mg (generic Xanax) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall was initiated voluntarily by the manufacturer.
A lot of LYFO-DISK quality control kit was found susceptible to Gentamicin Synergy when it should have been resistant. The 153 affected units were distributed worldwide.
BioPro is recalling Titanium MPJ toe implants because instructions and patient cards falsely claim the devices are compatible with MRI imaging, when safety testing for this titanium version has not been conducted.
Macleods Pharma USA is voluntarily recalling Olanzapine 10 mg tablets nationwide due to cGMP (current good manufacturing practices) deviations identified during manufacturing. The recall affects 3,672 bottles distributed across the United States.
Morton Grove Pharmaceuticals is recalling Dexamethasone Elixir USP 0.5 mg/5 mL nationwide due to unknown impurities found at higher than permissible levels in affected lots.
Triple E is recalling 2010-2014 Unity, Libero, and Serenity motorhomes because missing refrigerator exhaust deflectors allow heat to overheat the wood frame, posing a fire risk.
Daimler Vans USA is recalling 2,153 2021 Mercedes-Benz Sprinter vans because an incorrectly installed shim on the torsion bar may fail, causing loss of vehicle stability and increasing crash risk.
Daimler Vans USA is recalling 2017-2022 Mercedes-Benz Metris vehicles because insecure fuel hose connections may cause leaks, increasing fire risk.
Terex is recalling 2016-2021 OM, Optima-HRX, and TCX aerial devices because emergency stop controls may fail to stop all boom functions, increasing injury risk.
General Motors is recalling 2010-2017 GMC Terrain vehicles because headlight housings may reflect excessive light, causing glare for other drivers and increasing crash risk.
Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.
Yamaha is recalling 2021-2022 MT-09 and Tracer 9 GT motorcycles because improper ECU programming may cause engine stalls or limit throttle response, increasing crash risk.
Ubco is recalling 2021-2022 2X2 ADV motorcycles because a wheel hub gear may loosen and contact the motor, potentially causing the wheel to seize and increasing crash risk.
Mercedes-Benz is recalling 2020 AMG CLA 35 and 2021 GLA 250 vehicles because loose rear brake caliper fasteners may reduce braking performance or cause parts to detach.