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.

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.

24701–24725 of 79102

  • HighFDA (Food)·F-0099-2022·2021-11-10

    Picket Fence Creamery Ice Cream Recall: Undeclared Soy Lecithin

    Picket Fence Creamery is recalling CowaBrownie! ice cream in multiple sizes due to undeclared soy lecithin. Consumers with soy allergies should not consume this product.

    Product
    Picket Fence Creamery, Woodward, IA, CowaBrownie! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0188-2022·2021-11-10

    FDA Recalls 3M Red Dot ECG Monitoring Electrodes Due to Potential Carbon Stud Breakage

    3M Red Dot ECG monitoring electrodes (Catalog No. 2244) are being recalled due to potential breakage of the carbon stud from the eyelet. Approximately 2,081,000 units distributed nationwide and internationally are affected.

    Product
    3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6, SAP ID: 7100212989), packaged 10 electrodes per card, 5 cards per pouch, 20 pouches per shipper box, 1,000 electrodes total per shipper box. The 3M Red Dot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0095-2022·2021-11-10

    Pharmanex Kids Jungamals dietary supplement missing fish allergen label

    NSE Products, Inc. is recalling Pharmanex Kids Jungamals dietary supplement because the label does not disclose fish allergen present in the product's Vitamin E ingredient.

    Product
    Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0080-2022·2021-11-10

    Hamburger Buns Recalled for Listeria and Salmonella Contamination Risk

    Kansas City LLC., DBA Best Harvest Bakeries is recalling approximately 10,712 hamburger buns distributed to restaurants across 14 states due to positive environmental samples for Listeria and Salmonella.

    Product
    Hamburger buns, 4" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0110-2022·2021-11-10

    Picket Fence Creamery Cheese Curds Recall for Undeclared Wheat

    Picket Fence Creamery is recalling 12 oz packages of Taco White Cheddar cheese curds due to undeclared wheat and missing gluten-free labeling. The product was distributed to grocery stores in Iowa.

    Product
    Picket Fence Creamery, Woodward, IA, Taco White Cheddar cheese curds, Net Wt. 12 oz, UPC 094922414984
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0086-2022·2021-11-10

    Lupin Irbesartan Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan 75 mg tablets due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient. The recall affects 51,144 bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2022·2021-11-10

    Dental Implants Mislabeled as Smaller Size; Risk of Nerve Damage

    GM Helix Acqua Implant dental implants were mislabeled as a smaller size. If incorrectly installed in cases with low bone quality, they could damage the nerve or adjacent bone structures.

    Product
    GM Helix Acqua Implant 3.5x10, Article No. 140.944
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2022·2021-11-10

    Dental implant recalled due to size mismatch with labeling

    Implant Direct Sybron Manufacturing is recalling 83 dental implants from lot 166300 because the implants differ in size from what is labeled on the packaging. The implants were distributed across multiple US states and Japan.

    Product
    ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22013·2021-11-10

    ABUS MountZ Youth Helmets Recalled for Head Injury Risk

    ABUS is recalling about 790 MountZ youth helmets that do not meet U.S. safety standards for bicycle helmets. The helmets pose a risk of head injury and should be returned for a full refund.

    Product
    ABUS MountZ Youth Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0108-2022·2021-11-10

    Picket Fence Creamery Cheese Curds Recalled for Undeclared Soy

    Picket Fence Creamery is recalling Bacon-Ranch White Cheddar cheese curds due to undeclared soy lecithin. The product may pose a risk to consumers with soy allergies.

    Product
    Picket Fence Creamery, Woodward, IA, Bacon-Ranch White Cheddar cheese curds, Net Wt. 12 oz, UPC 094922414984
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0100-2022·2021-11-10

    Picket Fence Creamery Mocha Ice Cream Recalled for Undeclared Soy

    Picket Fence Creamery is recalling Mocha! ice cream in multiple sizes due to undeclared soy lecithin. Consumers with soy allergies who purchased this product should not consume it.

    Product
    Picket Fence Creamery, Woodward, IA, Mocha! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0098-2022·2021-11-10

    Picket Fence Creamery Cow Path Ice Cream Recall Due to Undeclared Peanuts

    Picket Fence Creamery is recalling Cow Path ice cream because it contains undeclared peanuts, even though the label only declares nuts in general. Consumers with peanut allergies may be at risk.

    Product
    Picket Fence Creamery, Woodward, IA, Cow Path ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0197-2022·2021-11-10

    Dental implants recalled for size mismatch with package labeling

    Implant Direct is recalling 61 dental implants because the packaged implants are a different size than declared on the labeling. Patients who may have received these implants should contact their healthcare provider.

    Product
    ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2022·2021-11-10

    MEDRAD Twist & Go Syringe Recalled Due to Labeling Error

    Bayer Medical Care is recalling 6,950 units of MEDRAD Twist & Go Disposable Syringes due to labeling errors that could cause confusion about syringe compatibility with the MEDRAD Mark 7 Arterion Injection System.

    Product
    The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a syringe made from a clear polycarbonate material and is an accessory to the MEDRAD Mark 7 Arterion Injection System. It is designed to be loaded into the injector head of the injection system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0097-2022·2021-11-10

    Picket Fence Creamery Chocolate Malt Ice Cream Recall

    Picket Fence Creamery L.L.C. is recalling Chocolate Malt ice cream in multiple container sizes distributed to Iowa grocery stores due to undeclared soy lecithin, a potential allergen.

    Product
    Picket Fence Creamery, Woodward, IA, Chocolate Malt ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0083-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/80 mg) because the product was manufactured using an excipient that failed to meet conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0090-2022·2021-11-10

    Starbucks Doubleshot Espresso canned coffee recall due to sealing defect

    PepsiCo is recalling Starbucks Doubleshot Espresso canned coffee products due to inadequate sealing that may lead to premature spoilage. The recall affects approximately 85,956 cases distributed nationwide.

    Product
    Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 FL OZ UPC 012000008801
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/20 mg) nationwide because the product was manufactured using an excipient that failed conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0084-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed conductivity specifications. The recall affects 11,590 bottles of 30-count and 3,585 bottles of 90-count packages distributed nationwide.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0202-2022·2021-11-10

    Aspiration Syringe Kit MVSK60 Inadvertently Shipped with OUS Labeling

    MicroVention's Aspiration Syringe Kit (REF: MVSK60) was labeled for international distribution but inadvertently shipped to U.S. customers. The affected lot (H2146461) was distributed to Alabama, Nevada, and New York.

    Product
    Aspiration Syringe Kit, REF: MVSK60
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0107-2022·2021-11-10

    Picket Fence Creamery Orange Pineapple Ice Cream Recalled for Undeclared Yellow #6

    Picket Fence Creamery L.L.C. is recalling Orange Pineapple ice cream sold in Iowa because it contains undeclared Yellow #6, a color additive that may affect consumers with sensitivity to artificial dyes.

    Product
    Picket Fence Creamery, Woodward, IA, Orange Pineapple ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0159-2022·2021-11-10

    Ivar's Clam Chowder Recalled for Plastic Fragment Contamination

    Ivar's Kettle Classic Clam Chowder with Uncured Bacon is being recalled due to the presence of plastic fragments in the product. The recall affects approximately 14,968 sleeves distributed across thirteen Midwestern states.

    Product
    Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and packaged in 24 oz. clear plastic cups, in a double pack surrounded by a printed paperboard sleeve (2/24 cups per sleeve). Retail package's UPC 0 30383 19649…
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-0085-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling 696 bottles of Ezetimibe and Simvastatin Tablets (10 mg/40 mg) distributed nationwide due to failed excipient specifications and the presence of foreign tablets in bottles.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0088-2022·2021-11-10

    Irbesartan 300 mg tablets recalled for impurity in active ingredient

    Lupin Pharmaceuticals is recalling Irbesartan 300 mg tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects approximately 119,544 bottles distributed nationally.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0201-2022·2021-11-10

    Medtronic Neuromodulation Clinician Programmer Application Software Anomaly Recall

    Medtronic recalled the Clinician Programmer Application (CPA) model A610 due to a potential software anomaly. Affected versions 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 have been distributed worldwide. No illnesses or injuries have been reported.

    Product
    Clinician Programmer Application (CPA) model A610 Clinician Software Application
    Category
    Medical Device
    Distribution
    Distributed nationwide