State
72,820 recalls have nationwide distribution and so reach Iowa. 5,581 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,581 recalls naming Iowa we have scored against our rubric, 909 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,581 recalls whose distribution notice names Iowa specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Lupin Pharmaceuticals is recalling Clobetasol Propionate Cream 0.05% because it failed content uniformity specifications. The recall covers 5,082 tubes distributed nationwide.
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
American Contract Systems Inc is recalling 30 units of Convenience Kits containing Medline catheters because samples failed performance specifications.
Medline is recalling 45 Trach Tube Kits (SKU DYKM2330) due to a component labeling discrepancy. The recall covers units distributed in California.
American Contract Systems Inc is recalling 30 units of Convenience Kits because Medline catheters failed performance specifications.
AVID Medical, Inc. is recalling 130 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
American Contract Systems Inc is recalling 12 Convenience Kits containing Medline catheters because samples failed performance specifications.
Apotex Corp. is recalling 6,972 bottles of Paxil CR 37.5mg tablets because the product failed dissolution specifications and 24-month stability testing.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 150 mcg tablets because they may contain less active ingredient than labeled.
Storyteller Overland is recalling 2026-2027 MODE and 2026 GXV HILT vans because a rooftop fan component may overheat, increasing the risk of a fire.
PACCAR is recalling 2027 Peterbilt 548 trucks because incorrect front brake valve and hose sizes may delay brake response, increasing crash risk.
Chrysler is recalling 328,381 Jeep Grand Cherokee vehicles because rear coil springs may detach while driving, increasing crash risk.
Chrysler is recalling 2025-2026 Ram 1500 vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.
Forest River is recalling certain 2024-2025 transit buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.
FCA US is recalling specific 2024-2026 Jeep models because a software error may prevent the tire pressure monitoring system from detecting low pressure or illuminating the warning light.
Chrysler is recalling 2025-2026 Voyager and Pacifica vehicles because a cracked sensor capacitor may cause a loss of electronic stability control, increasing crash risk.
Forest River is recalling 2027 Vibe recreational trailers because the furnace exhaust may not be correctly attached, allowing carbon monoxide to build up inside the cabin.
Light Boy is recalling 2020 and 2023 GBX12SK light towers because the trailer frame may bend, causing the tower to detach and become a road hazard.
Tesla is recalling 2026 Model Y vehicles because front suspension fasteners may not be properly tightened, which could cause a loss of vehicle control.
Tiffin is recalling 2026-2027 Wayfarer recreational vehicles because the liquid propane tank may lack a remote shut-off or be loose, posing fire and crash risks.
Blue Bird is recalling 2025-2027 Vision school buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.
Jayco is recalling 2026-2027 Entegra and Seneca recreational vehicles because the tire size on the certification label may be incorrect, which could lead to installing the wrong replacement tires.
Jayco is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles due to a taillight harness defect that may cause incorrect warning lights on the instrument panel.