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.
Airstream is recalling 2017-2020 Basecamp trailers because the tire placard lacks spare tire information, which may lead to installing the wrong size tire.
Meritor is recalling specific steer axles because insufficient lubrication may damage wheel end bearings, potentially causing wheel separation and loss of vehicle control.
Keystone RV Company is recalling 2018-2020 Fuzion 429 recreational trailers because a pinched wiring harness may short circuit and cause a fire.
Transfer Flow is recalling rear brake lines for mobility van conversions due to incorrect tube nut fittings that may cause a pressure drop in the braking system.
BMW is recalling 2019 X7 xDrive40i and xDrive50i vehicles because the driver and passenger head air bags may not be properly aligned, potentially impairing deployment and increasing injury risk.
General Motors is recalling 2016-2019 Chevrolet Express and GMC Savana vehicles because rear-quarter windows may use tempered glass instead of laminated glass, increasing injury risk in crashes.
Jaguar Land Rover is recalling 28,671 2016 Range Rover and Range Rover Sport vehicles because a stuck spring may leave the left door unlatched, increasing crash risk.
DICK'S Sporting Goods is recalling Ethos Pull-Up Assist equipment because a plastic clip can break, posing a laceration hazard. Seven reports of equipment breaking resulted in six lacerations.
Revelate Designs is recalling 2019 Terrapin System 14L bicycle seat bags because straps can detach and entangle in the rear wheel, posing crash and injury risks.
Audi is recalling 2016-2018 Q3 vehicles with LED headlights because a broken front turn signal may not alert the driver, increasing crash risk.
Far East Brokers is recalling Fabulous Home Pineapple Corer & Slicers because the metal blade can detach, posing a laceration hazard.
D.B.P. Distribution is recalling Titanium 4000 capsules because they contain undeclared sildenafil and tadalafil and were marketed without an approved NDA or ANDA.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Aurora Packing Company is recalling approximately 62,112 pounds of raw beef products that may be contaminated with E. coli O157:H7. The products were shipped nationwide for further distribution and processing.
AmeriHerb International Inc is recalling 1 lb bags of dried dill weed potentially contaminated with E. coli. The product was distributed nationwide and to Canada.
Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling Curved Intraluminal Staplers, Model CDH25A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Preferred Pharmaceuticals is recalling Losartan Potassium 50mg tablets because FDA testing found an impurity above acceptable levels.
AmeriHerb International Inc is recalling 144 lbs of Mullein leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Newmar is recalling 2019 Mountain Aire and Essex motorhomes because loose brake caliper mounting bolts may reduce brake effectiveness and increase crash risk.