State
72,986 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,556 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 9,556 recalls whose distribution notice names Indiana specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The AXIOS Stent and Delivery System is being recalled because the outer sheath can detach and prevent proper stent expansion, requiring device replacement during the procedure.
Edifier speakers in Draeger's Infinity Central Station may not produce audible alarms when in analog mode, potentially delaying patient treatment. Approximately 1,013 units are affected worldwide.
The HOT AXIOS Stent delivery system's outer sheath tip may detach during use, preventing proper stent expansion and requiring device exchange. Boston Scientific is recalling 1,102 units distributed nationwide.
Boston Scientific recalls 1,399 units of AXIOS stent delivery systems due to outer sheath detachment that can prevent proper device expansion, requiring procedure prolongation and device exchange.
Karl Storz Endoscopy is recalling its Pediatric Uretero-Renoscope 7.3 Fr. due to unapproved reprocessing instructions. The device instructions contain procedures not reviewed or approved by the FDA for safety and efficacy.
Boston Scientific's HOT AXIOS stent delivery system may have an outer sheath that detaches and prevents proper stent expansion. The defective tip can remain around the stent, requiring device exchange during the procedure.
Boston Scientific is recalling 1,144 AXIOS Stent Delivery System units because the outer sheath's distal black tip can detach. If this occurs, the tip may remain around the stent saddle and prevent proper stent expansion, requiring device exchange.
Boston Scientific's AXIOS Stent Delivery System is being recalled because the outer sheath can detach during use, preventing proper stent expansion and requiring device exchange.
Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.
The W.S. Badger Company is recalling Badger 50 mineral sunscreen tins lacking the complete drug facts label, barcode, and directions for use. The recall affects 4,834 tins distributed nationwide.
Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.
Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.
New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.
Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.
Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.
Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.
Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.
Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.
AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.
Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.
Johnson Health Tech North America is recalling approximately 12,885 Matrix-brand Training Cycles due to seats that can unexpectedly lower during use. The company received 63 reports, including two falls, but no injuries have been reported.
Brinkley RV is recalling certain 2024-2025 Model G fifth wheel trailers because the solar charge controller may fail and overheat, increasing the risk of fire.
AliExpress is recalling about 980 Multi Styler Hair Dryers sold online from May 2023 through November 2024 because they lack an immersion protection device and pose an electrocution hazard if they fall into water while plugged in.
Cabinet Health is recalling about 65,000 refillable 4 oz. medicine bottles. The plastic lids can degrade with repeated use, losing child-resistance and posing a poisoning risk if children access the contents.
Greater Goods digital kitchen scales with easily accessible lithium coin batteries violate federal safety regulations due to missing child-resistant packaging and warnings. Ingestion of coin batteries can cause serious injury or death; no incidents have been reported.