State
73,388 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,587 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 9,587 recalls whose distribution notice names Indiana specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
St. Jude Medical's Merlin PCS 3650 programmer software may display overestimated predicted battery longevity for certain pacemakers. This could affect clinical decision-making regarding device maintenance and replacement timing.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Daytime dietary supplement due to use of an unapproved acidification process. The product was distributed to 42 states in approximately 34,526 cases.
Craftmatic Industries is recalling the Model 1 Base for Dual Bed Configurations due to a potential for the bed bases to separate or slip apart. This defect could cause dual-configured beds to shift unexpectedly.
Dental Choice is recalling 708 units of the CustMbite Model CBT-SRS-UL device nationwide because it was marketed and sold without FDA clearance.
Craftmatic Industries recalls the Legacy Base for Dual Bed Configurations due to a potential for beds to separate or slip away from one another. The defect poses a risk of unintended bed movement.
Thor Motor Coach is recalling 2022-2023 motorhomes whose electric retractable awning may drop due to a failing welded seam. This increases the risk of injury.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Combo Pack because the acidified/low acid dietary supplement was manufactured without an FDA-approved process.
Procter & Gamble is recalling Vicks ZzzQuil Liquid Melatonin Syrup Pediatric because it was manufactured without FDA's approved process for acidified/low-acid dietary supplements.
Neotract Inc is recalling 18,722 UroLift Systems due to potential improper implant deployment during use. Patients should contact their healthcare provider.
Malvern Panalytical is recalling 507 NanoSight NS300 units due to noncompliance with Class 1 laser safety requirements. The device may not meet established safety standards for laser-based instruments.
Lexus is recalling 2020-2022 RC F vehicles because the tire information label lacks the vehicle's weight capacity, which may increase crash risk.
Navistar is recalling certain 2023 IC CE school buses because the engine control module may experience an internal electrical short-circuit, causing the engine to stall unexpectedly. An unexpected engine stall increases the risk of a crash.
Turbett Surgical, Inc. is recalling the Turbett Surgical Container TS1500 because the affected units were subject to unapproved rework processes. Seven units were distributed to healthcare facilities in Colorado, Florida, North Carolina, and Pennsylvania.
Medtronic Sprinter OTW Model SPR2512W balloon catheter has incorrect balloon diameter printed on the Luer connection point: 2.25mm instead of correct 2.5mm. Correct specification appears on outer packaging.
Medline Micro-Kill Germicidal Bleach Wipes are being recalled nationwide due to stability failure affecting approximately 6.1 million wipes across multiple lot numbers.
Boston Scientific is recalling 10 units of the EkoSonic Kit endovascular device due to product mislabeling. Affected devices were distributed to medical facilities in 10 US states.
Boston Scientific is recalling 10 EkoSonic Endovascular Device Kits due to mislabeling. The affected kits were distributed to healthcare facilities in 10 U.S. states.
Glenmark Pharmaceuticals is recalling Tacrolimus Ointment 0.1% because tubes may split at the side seam. The recall affects over 654,000 units distributed nationwide.
Nissan is recalling specific air bag inflator replacement parts installed in Infiniti and Nissan vehicles due to a risk of explosion from propellant degradation.
KME is recalling 2021-2022 Predator and Panther fire trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.
Bowlus is recalling 2021-2022 Terra Firma and Endless Highways trailers because improperly connected LPG service valves may cause propane leaks and fire.
Grand Design is recalling certain 2022-2023 travel trailers because the electric awning's fabric seam may separate, allowing the awning to drop beyond normal operation and increase injury risk. Dealers will repair or replace the awning at no charge.
Volvo Trucks North America is recalling 2023 Volvo VN vehicles because the engine control module may short-circuit, causing the engine to stall and increasing crash risk.
Mack Trucks is recalling 2023 MD6/7 trucks because the engine control module may short-circuit, causing unexpected engine shutdowns that increase crash risk.
Keystone and Dutchmen travel trailers from 2022-2023 have awnings whose fabric may separate at the welded seam, causing the awning to drop. Dealers will repair or replace the awning free of charge.