The Recall Desk

State

Iowa product recalls

73,509 recalls have nationwide distribution and so reach Iowa. 5,593 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,593
Critical
910
Severe
1,591
Most recent
2026-10-24

Of the 5,593 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 1,591 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,593 recalls whose distribution notice names Iowa specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24426–24450 of 79102

  • LowFDA (Drugs)·D-0264-2022·2021-12-08

    Tydemy Oral Contraceptive Recalled Due to Subpotent Drug

    Lupin Pharmaceuticals has recalled Tydemy oral contraceptive tablets nationwide due to subpotency. The recall affects 4,113 cartons distributed throughout the United States.

    Product
    Tydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets, 0.451 mg), packaged in cartons containing 3 wallets of 28 Tablets each, Rx Only, Distributed by: Lupin Pharmaceuticals, Inc., Baltimore, Maryland…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V943000·2021-12-07

    Great Dane Recalls 2022 Trailers Due to Wheel Hub Lubrication Defect

    Great Dane is recalling 2022 Champion and Everest trailers because insufficient wheel hub lubrication could cause bearing failure and loss of control.

    Product
    GREAT DANE — GREAT DANE CHAMPION, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22025·2021-12-06

    Drive DeVilbiss Adult Bed Rails Recalled; Two Deaths from Entrapment

    Drive DeVilbiss Healthcare is recalling four models of adult portable bed rails that can trap users between the rail and mattress, causing asphyxiation. Two deaths have been reported.

    Product
    Bed Assist Handles and Bed Assist Rail
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·046-2021·2021-12-05

    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Listeria

    Alexander & Hornung is recalling approximately 2.3 million pounds of fully cooked ham and pepperoni products due to possible Listeria monocytogenes contamination.

    Product
    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·045-2021·2021-12-03

    Erie Meat Products Recalls Chicken Bologna Imported Without Inspection

    Erie Meat Products Ltd. is recalling approximately 1,224 pounds of chicken bologna imported into the U.S. without FSIS reinspection. The products were distributed to correctional institutions in four states.

    Product
    Erie Meat Products Ltd. Recalls Chicken Bologna Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V940000·2021-12-03

    Zero Motorcycles Recalls 2022 SR Models Due to Incorrect Rear Brake Pads

    Zero Motorcycles is recalling 2022 SR, SR/F, and SR/S motorcycles because incorrect rear brake pads were installed, which may not work as intended and increase crash risk.

    Product
    ZERO — ZERO SR/F, SR, SR/S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V937000·2021-12-02

    2021 Hyundai Accent brake master cylinder defect recall

    Hyundai is recalling certain 2021 Accent vehicles due to a brake master cylinder defect. The component may have sharp edges that damage the inner oil seal, reducing braking performance and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V938000·2021-12-02

    2022 Hyundai Tucson: Inoperative Headlights and Taillights from Software Defect

    Hyundai is recalling 2022 Tucson vehicles with incompatible ICU software that can disable headlights and taillights, reducing visibility and increasing crash risk. All affected vehicles have been repaired.

    Product
    HYUNDAI — HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V939000·2021-12-02

    2021 Acura RDX Driveshaft Defect May Cause Loss of Drive Power

    Honda is recalling certain 2021 Acura RDX vehicles because the front driveshaft may have been improperly heat-treated, potentially causing driveshaft failure and sudden loss of drive power or vehicle rollaway.

    Product
    ACURA — ACURA, HONDA RDX, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E099000·2021-12-01

    Cummins Recalls X12 Diesel Engines Due to Fuel Tube Cracking Risk

    Cummins is recalling X12 Diesel Engines because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0214-2022·2021-12-01

    MaryRuth's Organic Infants Liquid Probiotic Recalled for Bacterial Contamination

    MaryRuth's Organic Infants Liquid Probiotic dietary supplement is being recalled because internal testing found Pseudomonas aeruginosa contamination. The affected product is distributed nationwide.

    Product
    MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7 Serving size (five drops - start with one and work up to 5) Organic Proprietary Probiotic Blend 250 mg. Bifidobacterium lactis Bifidobacterium infantis…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·22024·2021-12-01

    Halo Recalls Children's Projector Flashlights for Button Battery Hazard

    HALO Branded Solutions Inc. is recalling about 82,500 children's projector flashlights distributed in care packages because children can disassemble them and access button cell batteries, creating ingestion and choking hazards. Two incidents have been reported, including one requiring surgery.

    Product
    Projector Flashlights (included as part of a care package)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V934000·2021-12-01

    Mercedes-Benz Recalls 2021 Sprinter Vans for Rear Step Bolt Issue

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because improperly tightened rear step bolts could allow the step to separate, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 1500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22023·2021-12-01

    DEWALT Jobsite Pro Wireless Earphones Recalled for Burn and Fire Hazards

    E-filliate is recalling about 301,800 DEWALT Jobsite Pro Wireless Earphones because they can overheat during charging or use, posing burn and fire hazards. The company has received 61 reports of overheating, including five fires and four minor burn injuries.

    Product
    DEWALT ® Jobsite Pro Wireless Earphones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V933000·2021-12-01

    2021 Mercedes-Benz Sprinter Vehicles Recalled for Brake Hose Damage Risk

    Daimler Vans USA is recalling 2021 Mercedes-Benz and Freightliner Sprinter vans because the front fender liner may damage the brake hose, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 4500, SPRINTER 3500, SPRINTER 2500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V936000·2021-12-01

    Kia Rio 2020–2021 brake master cylinder defect recall

    Kia Motors recalls 2020–2021 Rio vehicles due to brake master cylinder manufacturing defects that can reduce braking performance. The defect may cause longer pedal travel and extended stopping distance, increasing crash risk.

    Product
    KIA — KIA RIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0289-2022·2021-12-01

    CT Scanner Software May Cause Workflow Delays and Patient Rescans

    Siemens SOMATOM Edge Plus CT scanners with syngo.CT VB20 software may experience workflow interruptions, potentially delaying diagnoses and requiring patient rescans. The issue affects 64 units nationwide.

    Product
    SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0276-2022·2021-12-01

    Diagnostic thromboplastin reagent recalled due to performance issues

    Instrumentation Laboratory is recalling HemosIL ReadiPlasTin diagnostic reagent kits due to performance issues including imprecision and out-of-range quality controls that could result in inaccurate test results.

    Product
    HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0293-2022·2021-12-01

    Medtronic Wireless Recharger for InterStim Micro May Become Unresponsive

    Medtronic's wireless recharger for the InterStim Micro implantable neurostimulator may become unresponsive if charging procedures from the user guide are not followed. Approximately 10,081 devices are affected nationwide.

    Product
    Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the InterStim Micro (Model 97810) implantable neurostimulator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0292-2022·2021-12-01

    Medtronic Endurant IIs stent graft recalled due to spindle detachment risk

    Medtronic recalls 419 Endurant IIs stent grafts due to risk of spindle detachment from the hypotube during deployment.

    Product
    Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0282-2022·2021-12-01

    Medtronic Cardiac Device Software Affected by Data Processing Error

    Medtronic is recalling software used in certain cardiac implant devices due to a data processing error that may fail to collect episode data. Approximately 18,715 devices are affected worldwide.

    Product
    Medtronic CareLink SmartSync Device Manager application software (D00U005) used by the following Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds): Cobalt XT VR: DVPA2D1, DVPA2D4; Cobalt VR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0241-2022·2021-12-01

    Philips CombiDiagnost R90 X-ray systems missing required radiation warning labels

    Philips Healthcare is recalling CombiDiagnost R90 X-ray systems because some units lack required FDA radiation warning labels and X-ray certification statements. No injuries have been reported.

    Product
    CombiDiagnost R90 is multi-functional general R/F systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide