State
73,827 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 276 Basic Setup Packs because the Medtronic gloves inside may have splits or holes that compromise sterility.
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) 30 mg capsules because they failed to meet dissolution specifications.
Sun Pharmaceutical Industries is recalling specific lots of Alfuzosin Hydrochloride Extended-release Tablets because a consumer complaint identified a broken piece of wire rope embedded in a tablet.
Amerisource Health Services is recalling 454 cartons of Cyclosporine Capsules, 100 mg, due to failed impurity specifications.
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The affected lot is distributed nationwide.
MED-EL is recalling 538 SONNET Mini Battery Pack Cables because the compartment lock was not firmly welded to the housing.
Siemens is recalling specific Calibrator A kits due to confirmed negative bias and potential calibration failures for the FT4 assay on certain ADVIA Centaur systems.
Dr. Reddy's Laboratories is recalling specific lots of Zenatane (isotretinoin) 20 mg capsules because they failed to meet dissolution specifications.
Becton Dickinson is recalling specific lots of the BD AffirM VPIII Microbial Identification Test because blue speckles or fibers may cause invalid test results.
Siemens recalls ADVIA Centaur Calibrator A kits due to negative bias in FT4 assays and potential calibration failures on specific systems.
Allegiant Health is recalling HealthA2Z Chewable Aspirin 81 mg because rubber particles were found in the bulk product.
L. Perrigo Company is recalling Salicylic Acid Cream, 6%, due to an out-of-specification organic impurity. The FDA classified this as a Class III recall.
L. Perrigo Company is recalling Salicylic Acid Shampoo, 6%, because the active ingredient failed impurity specifications.
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The recall covers 4,404 cartons distributed nationwide.
Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because a driveshaft bracket may not be properly welded, posing a fire risk in a crash.
Zero Motorcycles is recalling 2017 S, DS, and FXS motorcycles because the Anti-Lock Braking System may function improperly, increasing crash risk.
Rexon is recalling about 46,000 Craftsman portable table saws sold at Sears because the stand can collapse, posing laceration and impact injury risks.
Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vans because the Blind Spot Monitoring system does not work due to incompatible parts.
H&H Sports Protection is recalling TORC T-55 V2 half helmets because they may not adequately protect the wearer or stay secured during a crash.
L.L. Bean is recalling Adventure Adjustable Snowshoes because the plastic deck can weaken and break, posing a fall hazard. No injuries have been reported.
Keystone is recalling 2017 Cougar and Laredo recreational trailers that may have two carbon monoxide detectors instead of a smoke detector, increasing fire injury risk.
Fiat is recalling 2017 500X vehicles because the tire pressure warning light may not illuminate when tires are underinflated, increasing crash risk.
Forest River is recalling 2017 Prime Time Crusader recreational trailers because the Federal placard incorrectly lists axle capacity as 7,000 lbs instead of 6,000 lbs, which could lead to overloading.