State
72,940 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,555 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 9,555 recalls whose distribution notice names Indiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 11,200 ANNQUAN power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded.
About 650 Schwinn Ovation Bicycle Child Carriers are being recalled because the buckles securing the restraints around the child can release during use, posing a fall hazard.
About 50,330 jars of Mamisan Pain Relieving Topical Ointment are being recalled because the ointment contains lidocaine and the packaging is not child-resistant.
About 80 SereneLife above-ground pools 48 inches and taller, models SLPORND15 and SLPORND18, are being recalled because a compression strap may create a foothold allowing a child to access the pool.
About 12,000 JOKOSIS portable bed rails, model HC0262, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 2,800 17 Stories Furniture 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
International Motors is recalling 2026-2027 IC Bus CESB school buses because wheelchair retractors may not lock, increasing injury risk.
Subaru is recalling certain 2026 Forester vehicles because the rear hatch support bracket may detach without warning, allowing the rear hatch to fall unexpectedly and increase injury risk.
Ford is recalling certain 2025 and 2026 Maverick vehicles because the instrument panel cover may separate during an airbag deployment, potentially striking occupants and increasing injury risk.
Altec is recalling certain 2023-2025 Aerial Device and Digger Derrick vehicles because the electronic taillight module harness may have inadequate circuit protection.
About 260 Currey & Company Electra chandeliers are being recalled because the component connecting the fixture to the ceiling mount is not threaded properly and the fixture can fall.
General Motors is recalling 2025–2026 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not produce sufficient volume change between stopped and low-speed operation, failing to meet federal safety standards.
Honda is recalling 2024–2026 CBR600RR motorcycles because the cylinder head may have been improperly manufactured, risking rear wheel lockup and engine fire.
International Motors is recalling 2026 IC Bus CECB vehicles because wheelchair retractors may fail to lock, increasing injury risk during transit.
Ford is recalling certain 2021-2022 Bronco vehicles previously repaired under recall 23V165, because the rearview camera image may still be displayed after a backing event has ended.
Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,603 cases of loose bulk peppermint peaches over potential contamination with Listeria monocytogenes, under enforcement record H-0323-2026.
Moonlight Packing is recalling a further 2,622 cases of loose bulk peppermint peaches over potential Listeria monocytogenes contamination, under enforcement record H-0324-2026.
Moonlight Packing is recalling 237,656 cases of loose bulk yellow peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 483,973 cases of 4 lb packaged yellow peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen jamun after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 13,069 cases of 4 lb Peppermint Peach white peaches over potential contamination with Listeria monocytogenes.
Moonlight Packing is recalling 46,048 cases of 2 lb bagged peaches, including Kroger-distributed packs, over potential contamination with Listeria monocytogenes.
Chetak New York is recalling Deep-brand frozen surti papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.