State
20,324 recalls have nationwide distribution and so reach Iowa. 0 additional recalls listed Iowa specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Iowa consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.
BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.
Mockingbird LLC is recalling about 25,390 Single Strollers because the lower side of the frame can crack, posing a fall risk to children. The company is offering a free frame reinforcement kit.
Polaris is recalling model years 2021–2023 Sportsman 450 and 570 ATVs because an improperly assembled wiring harness can contact the brake line and vehicle frame, resulting in front brake loss and fire.
Sunbeam Queen Size Heated Blankets (model 32810027) can overheat, posing fire and burn hazards. The firm has received 13 reports of overheating with no injuries reported. Consumers should stop using them immediately and contact Star Elite for a refund.
Ecoxall is recalling sodium hydroxide and potassium hydroxide products sold on Amazon because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act. The products pose a risk of chemical burns and skin or eye irritation.
STIHL is recalling about 2,700 iMOW docking stations that can short-circuit when exposed to moisture, creating a fire hazard. Eight reports of thermal overheating and two fires have been reported; no injuries.
IKEA is recalling LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration risk. About 22,400 units in the U.S. are affected.
Fredericksburg Farms is recalling about 6,500 scented candles with glass lids because some lids are too tight, causing jars to break when forcibly opened. The company has received four reports of hand lacerations.
Pfizer is recalling Nurtec® ODT (rimegepant) 75mg tablets because the blister card packaging is not child-resistant as required by law, posing a poisoning risk to children who may access and swallow the contents.
The Cardiosave Rescue intra-aortic balloon pump may suddenly stop working due to communication failure between internal circuit boards, interrupting patient therapy and threatening hemodynamic stability.
Snowy Range Blue hand sanitizer is recalled due to FDA findings of methanol, acetaldehyde, and acetal above permissible limits. The product was distributed nationwide across all lot codes.
Chukar Cherry Company is recalling Cherry Bombs Bits 'n Pieces chocolate candy nationwide due to undeclared hazelnuts, a food allergen.
Datascope Corp. is recalling Cardiosave Hybrid IABP devices due to a connection failure that may cause unexpected shutdown during use. The failure prevents communication between the device's display head and base unit.
The Cardiosave Hybrid intra-aortic balloon pump (IABP) is being recalled because it may unexpectedly shut down due to communication loss between internal components. The shutdown could interrupt therapy in cardiac patients and compromise their hemodynamic stability.
Pharmedica USA recalled Purely Soothing 15% MSM Drops nationwide due to non-sterility concerns. The voluntary Class I recall affects approximately 1,904 bottles distributed via e-commerce and trade shows.
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to a coiled cord cable connection failure that may cause unexpected device shutdown and loss of communication.
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to helium regulator failures that may cause insufficient helium levels when the pump console is docked. The defect may affect device operation.
Select CardioMEMS CM2000 PA sensors may operate outside their intended frequency range above 2,000 feet elevation, potentially causing inaccurate readings or signal acquisition problems in heart failure monitoring.
CardioMEMS heart-failure monitoring devices are recalled due to radiofrequency emissions that can interfere with other medical devices like pacemakers when operating nearby.
Carefusion's CD5 Series Genesis surgical sterilization containers are being recalled due to failure to meet shelf-life testing requirements, resulting in a potential breach of sterility. The recall affects 5,952 devices distributed worldwide.
Apotex Corp. is recalling Brimonidine Tartrate eye drops (67,056 bottles nationwide) because cracks in bottle caps may compromise sterility and expose patients to contamination.
Covidien is recalling certain Tri-Staple 2.0 surgical stapler reloads due to a mechanical defect that may cause the device to malfunction during surgery. Affected units may fail to form staples properly, potentially causing serious surgical complications.
B. Braun Medical Inc. is recalling Heparin Sodium in Dextrose Injection (Lot J2C017) due to subpotent anti-Factor IIa activity, which may reduce anticoagulant effectiveness.
Shirakiku brand Chili Pepper Powder (ICHIMI TOGARASHI) is being recalled nationwide and internationally because it contains sesame that is not declared on the ingredient label. Consumers with sesame allergies should not consume this product.