State
73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 11 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used, potentially leading to corrosion.
AngioDynamics is recalling 7,348 Solero Microwave Tissue Ablation applicators to update manuals and software, reducing the risk of patient harm from procedure delays.
Bio-Rad Laboratories is recalling 5,212 units of MRSASelect in vitro diagnostic plates due to abnormal agar coloration and non-characteristic colony growth.
I.T.S. GmbH is recalling 65 titanium rim plates because they have the wrong article number laser marked on them. The devices were distributed in the US and several international countries.
Smiths Medical ASD Inc. is recalling JELCO Hypodermic Needles with incorrect length and gauge. The recall covers 109,000 units distributed nationwide.
NxStage Medical is recalling specific lots of PureFlow B Solution because they were mislabeled with the incorrect product number.
Abbott is recalling Alinity c Cuvette Segments because individual cuvettes may seat lower than designed, potentially preventing the sample probe from making efficient contact with the cuvette bottom.
NxStage Medical is recalling 1,998 units of PureFlow B Solution because certain lots were mislabeled with the incorrect product number.
Microbiologics Inc is recalling 249 units of Cepheid Xpert MRSA/MRSA NxG and Xpert SA Nasal Complete Control Panels because they have an incorrect shelf life.
Microbiologics is recalling 235 units of Cepheid Xpert SA Nasal Complete Control Panels due to incorrect shelf life labeling.
Smiths Medical ASD Inc. is recalling 7,840 Portex Blue Line Ultra Tracheostomy Tubes because they were packaged with an incorrect size inner cannula.
Fresenius Medical Care is recalling 257 units of the 2008T BlueStar hemodialysis machine due to a power logic board fail message on software version 2.72.
Daimler Trucks North America is recalling 2019-2020 Freightliner M2 and 2020 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.
Keystone is recalling 2020 Crossroads Cruiser fifth wheel trailers because the furnace exhaust vent may be missing, creating a carbon monoxide risk.
Daimler Trucks North America is recalling specific Thomas Built Buses school buses because the driver-side rear brakes may drag, increasing the risk of smoke and fire.
Godwin is recalling 2017 dump bodies equipped with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.
LA West is recalling 2018-2019 Ford Transit vehicles with modified glass roof hatches that may shatter due to stress, posing an injury risk.
Vac-Tron is recalling 2015-2019 LP 873 SD trailers that may lack required lights and reflectors, increasing crash risk at night.
Unicell is recalling 325 commercial vehicles equipped with ASA Electronics Voyager monitors that may display reversed back-up camera images, increasing crash risk.
Amazon is recalling AmazonBasics 1500 Watt Ceramic Space Heaters because they can overheat, posing fire and burn hazards. Consumers should stop using the heaters and contact Amazon for a full refund.
Target is recalling Cat & Jack 'Lilia' toddler rain boots because the unicorn horn can detach, posing a choking hazard to young children.
Entegra is recalling 2020 Anthem and Cornerstone motorhomes because an insufficiently tightened steering shaft bolt may cause steering failure, increasing crash risk.
Cushy Form is recalling about 2,300 folding mattresses sold on Amazon.com because they fail to meet federal flammability standards, posing a fire hazard.
Chrysler is recalling 2019 Jeep Renegade vehicles with the Upland trim package because the occupant restraint controller may be miscalibrated, increasing injury risk in crashes.
Lakota is recalling 2018-2020 Colt horse trailers because a weak aluminum axle carrier may tear, affecting stability and increasing crash risk.