State
73,198 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,590 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 1,320 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
IKEA is expanding a recall of LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration hazard. No injuries have been reported.
Amer Sports Winter & Outdoor Company recalls certain Armada, Atomic, and Salomon ski touring bindings sold from May 2022 through September 2023 because the toe component can fail, causing the ski boot to disconnect and posing fall and injury risks.
Hino is recalling 2022-2023 NE7, NJ7, and NV7 trucks because the shift selector indicates a Park position that lacks a mechanical park mechanism, creating a rollaway risk.
Toyota Tundra trucks have an incorrect load-carrying capacity label that can result in vehicle overloading, increasing crash risk. Toyota will mail corrected labels free of charge to affected owners.
DR Power Equipment and Generac are recalling approximately 2,930 tow-behind field and brush mowers because the exhaust pipe can break from excessive heat, posing fire and burn hazards. The manufacturer has received 14 reports of fires damaging the mowers.
iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn hazard to children. About 13,300 units were sold between March and June 2023.
Subaru is recalling 2021-2023 Crosstrek, Forester, Legacy, and Outback vehicles. A weld defect in the inhibitor switch allows water to enter and cause the switch to fail, disabling reverse lights and camera display, increasing crash risk.
Textron Specialized Vehicles is recalling approximately 6,800 Arctic Cat Prowler Pro and Tracker Off Road 800SX side-by-side vehicles from model years 2022 and 2023 because they can roll away while parked on an incline.
Textron Specialized Vehicles is recalling about 1,660 E-Z-GO ELiTE Express and Tracker OX EV vehicles because internal motor wiring damage can cause the vehicle to move unintentionally, creating a crash hazard. One incident of unexpected movement has been reported but no injuries.
FreshPoint Bix Produce cantaloupes are being recalled due to potential Salmonella contamination. The recalled product was distributed to Iowa, Minnesota, North Dakota, and Wisconsin.
Braga Fresh Foods is recalling Wegman's Organics Sweet Kale Chopped Salad Kit due to undeclared egg allergen. The product was distributed nationwide and may pose a risk to individuals with egg allergies.
Cosmedent is recalling the FlexiCup Composite Finishing & Polishing System due to reports that the elastomer cup material is crumbling. Approximately 7,400 packs distributed worldwide are affected.
GlaxoSmithKline is recalling TUMS antacid tablets in Lot KH5L due to glass mineral wool contamination. Affected consumers should stop use immediately.
Nature's Path Organic Dark Chocolate Chip Waffles are recalled because peanuts were not declared on the label, posing a risk to consumers with peanut allergies.
Randox Laboratories is recalling the RX Daytona Plus (without ISE) IVD Clinical Chemistry Analyzer due to a flaw in rerun settings that may cause incorrect test result reporting.
Siemens Cios Alpha (VA30) C-arm X-ray systems have a software issue that may not meet updated DIN and IEC standards. This defect could result in patient misdiagnosis or unnecessary repeat imaging.
GlaxoSmithKline is recalling TUMS Antacid 1000 mg chewable tablets in Assorted Berries flavor due to glass mineral wool contamination found in some bottles. Product was distributed nationwide.
Select Custom Solutions is recalling JayRobb Vanilla Flavored Egg White Protein Powder due to plastic contamination. Approximately 1,008 pouches distributed nationwide are affected.
Covidien recalled 42,367 McGrath Mac 2 disposable laryngoscope blades due to an ineffective anti-fog agent that may cause screen condensation and visual obstruction during intubation procedures.
Coapt LLC is recalling the Dome Electrode Gen2 system due to potential burns or blistering from exposure to sunlight, warm temperatures exceeding 12 hours, or battery damage.
GlaxoSmithKline is recalling TUMS Antacid tablets (Lot HA7G, expiration 8/31/2027) due to contamination with glass mineral wool. The product was distributed nationwide.
Randox Laboratories is recalling 13 RX Monaco-IVD Clinical Chemistry Analyzers with a rerun feature defect that may report incorrect test results when samples are outside normal assay range. Units were distributed nationwide including Puerto Rico.
Sun Pharmaceutical is recalling 7,392 bottles of Liothyronine Sodium Tablets (Lot DND0058A) nationwide due to failed impurity and degradation specifications. Patients should contact their healthcare provider.
The RX Daytona Plus clinical chemistry analyzer may report incorrect results when samples fall outside normal range and the automatic rerun feature malfunctions. Randox Laboratories is recalling 5 units distributed nationwide.
Nova Biomedical Prime Plus Analyzers may report incorrect creatinine levels during the first 2-4 hours after installing a new sensor cartridge. These errors may not be identified by traditional quality control practices.