State
72,984 recalls have nationwide distribution and so reach Iowa. 5,585 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,585 recalls naming Iowa we have scored against our rubric, 910 (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 5,585 recalls whose distribution notice names Iowa specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Superb Sports baby bath seats sold on Amazon can tip over while in use, posing a drowning hazard to infants. No injuries have been reported.
AliExpress is recalling LVOE-brand hair dryers sold from April 2023 through December 2024 because they lack immersion protection and can cause electrocution if they fall into water while plugged in. No injuries have been reported.
About 21,250 DEWALT 70,000 BTU outdoor propane heaters are being recalled due to operating instructions that can prevent proper fan operation, causing overheating and fire and burn hazards. No injuries have been reported.
HONEYJOY Convertible and Foldable High Chairs are being recalled because they were marketed for infant sleep with an incline angle exceeding 10 degrees, violating federal safety regulations. About 2,750 units sold exclusively on Amazon from April 2023 to August 2024 are affected.
Sakar International is recalling about 199,000 Vivitar Blender Bottles sold at Target because the blades can continue operating when the bottle is removed from the base. No injuries have been reported.
AliExpress is recalling about 80 foldable travel hair dryers sold from April 2022 through January 2025 because they lack immersion protection and can cause electrocution or shock if they fall into water while plugged in. No injuries have been reported.
Nova Bus is recalling 2022-2023 LFS transit buses because high voltage battery hardware may come loose and cause a short circuit, creating a fire risk.
The CVAC Aspiration System requires a labeling update to add safety instructions for high-viscosity kidney fluid. Continuing fluid inflow without adequate outflow can create dangerous intrarenal pressure imbalances.
Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Neti Pot Nasal Wash System due to bacterial contamination with Staphylococcus aureus. Consumers should stop using this product immediately.
Hearthside Food Solutions is recalling approximately 489,887 pounds of ready-to-eat breakfast sandwiches because they contain sesame, a known allergen, that is not declared on the label.
Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System nationwide due to bacterial contamination with Staphylococcus aureus. Affected lot number is 024122661Al with expiration date 12/2027.
SinuCleanse Premixed Saline Packets sold nationwide are being recalled due to contamination with Staphylococcus aureus, a bacterium that can cause infection.
Jayco is recalling 2024-2025 Entegra Anthem, Aspire, and 2025 Reatta XL motorhomes because a fuel hose may separate, causing a leak, fire, or engine stall.
Medline procedure kits containing plastic syringes are recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health. The affected kits were distributed nationwide in the US and Canada.
Medline medical procedure kits containing plastic syringes are being recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health.
Medline is recalling General Endoscopy procedure kits due to plastic syringe defects that may leak or break. The affected kits pose potential risk to patient health during medical procedures.
Medline Industries is recalling 1,228 surgical procedure kits containing defective plastic syringes. The syringes may leak or break during use, potentially affecting patient safety.
Baxter is recalling 112 units of the TruSystem 7500 surgical table due to a software issue preventing upper back adjustment during emergency mode. No injuries have been reported.
Medline is recalling 1,958 delivery and labor procedure kits containing plastic syringes with leaks, breakage, and quality defects that may pose a risk to patient health.
Baxter TruSystem 7500 medical devices are affected by a software issue that prevents the upper back section from operating when emergency mode is enabled. Approximately 1,709 units have been recalled nationwide.
Medline is recalling 808 medical procedure kits containing plastic syringes with quality defects that may leak or break during use. Affected customers should stop using these kits and contact Medline for replacement instructions.
Medline is recalling certain arterial pressure monitoring line kits due to excess material on female luer fittings. The affected kits were distributed worldwide, including the United States.
Medline is recalling angiography and catheterization procedure kits containing plastic syringes that may leak or break. The recalled kits affect 1939 units distributed nationwide and in Canada.
Babyganics Sheer Blend SPF 50 Mineral Sunscreen is being recalled nationwide because ingredients separated during stability testing, prompting an FDA Class II recall.
Baxter is recalling 2 units of TruSystem 7500 Hybrid (MC) due to a software issue that disables the upper back section adjustment when emergency mode is activated.