The Recall Desk

State

Iowa product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25501–25525 of 79159

  • SevereFDA (Food)·F-0897-2021·2021-09-08

    BrightFarms Spinach Recall Due to Potential Salmonella Contamination

    BrightFarms Spinach packaged in 4oz and 8oz clamshells may be contaminated with Salmonella. The affected product was grown at the company's Rochelle, Illinois indoor farm and distributed across multiple Midwest states.

    Product
    BrightFarms Spinach; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0890-2021·2021-09-08

    BrightFarms Harvest Crunch Salmonella Contamination Recall

    BrightFarms Harvest Crunch packaged salad may be contaminated with Salmonella. The recall affects products distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.

    Product
    BrightFarms Harvest Crunch; packaged in clear plastic clamshells; 4oz; grown at the company's Rochelle, Illinois indoor farm
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0779-2021·2021-09-08

    MEDICALLY MINDED Hand Sanitizer Gel Recalled for Methanol Contamination

    Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (8.5 FL OZ) due to potential methanol contamination. The product was manufactured under the same conditions as a lot previously found to contain methanol.

    Product
    MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ (250 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0782-2021·2021-09-08

    MEDICALLY MINDED Hand Sanitizer Gel Recalled for Methanol Contamination

    Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (Ethyl Alcohol 70% v/v, 8.5 FL OZ / 250 mL) distributed nationwide due to manufacturing conditions that led to methanol contamination in product lots.

    Product
    MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1 ,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0778-2021·2021-09-08

    Hand Sanitizer Gel Recalled Due to Methanol Contamination Risk

    Global Sanitizers LLC is recalling MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel (70% ethyl alcohol) due to manufacturing deviations. Products were made under the same conditions as a lot found to contain methanol.

    Product
    MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera, (Ethyl Alcohol 70% v/v), 10 FL OZ / 300 mL, Manufactured by Grupo V-Klean S.A. de C.V, Calle Alborada 124, Parques del Pedregal, Tlalpan, 14250 Ciudad de Mexico, CDMX, Distributed by SBL Brands, LLC. Las Vegas, NV…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0901-2021·2021-09-08

    Cahill Cheddar with Porter Cheese Recalled for Listeria Contamination Risk

    Whole Foods Market is recalling Cahill Cheddar with Porter cheese (PLU 93579) sold in clear plastic packaging due to potential contamination with Listeria monocytogenes, a serious foodborne pathogen.

    Product
    Cahill Cheddar with Porter PLU 93579 packaged in clear plastic
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0896-2021·2021-09-08

    BrightFarms Mighty Romaine Recalled for Potential Salmonella Contamination

    BrightFarms is recalling Mighty Romaine lettuce sold in 4oz and 8oz clamshells because the product may be contaminated with Salmonella.

    Product
    BrightFarms Mighty Romaine; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0891-2021·2021-09-08

    BrightFarms 50/50 Spring & Spinach Salmonella Contamination Recall

    BrightFarms 50/50 Spring & Spinach in 4oz clamshells may be contaminated with Salmonella. The product was distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.

    Product
    BrightFarms 50/50 Spring & Spinach; packaged in clear plastic clamshells, 4oz; grown at the company's Rochelle, Illinois indoor farm
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2410-2021·2021-09-08

    COVID-19/Flu Rapid Test Distributed to Non-Certified Laboratories

    COVID-19/Flu rapid diagnostic test was distributed to laboratories not certified under federal clinical standards. The 563,290-unit recall affects nationwide distribution; products were authorized only for CLIA-certified laboratories.

    Product
    Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential Diagnosis of SARS-CoV-2, Influenzas Type A, and Type B Antigens Simultaneous qualitative detection and differentiation of nucleocapsid antigen from SARS-CoV-2, influenza A and influenza B directly from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0904-2021·2021-09-08

    Your Way Fresh Yogurt Parfait Recalled for Undeclared Soy

    Your Way Fresh Sliced Banana + Strawberry Yogurt Parfait is being recalled because the yogurt ingredient contains soy lecithin, but soy is not declared on the product label. Consumers with soy allergies may face serious health risks.

    Product
    Your Way Fresh, Sliced Banana + Strawberry Yogurt Parfait; Net wt. 6.25 oz (177 g); UPC 8 54426 00807 8; Distributed by Your Way Fresh, Newport Beach, CA, 12 cups per case;
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1016-2021·2021-09-08

    Rocky Top Farms Cherry Butter recalled for undeclared milk allergen

    Rocky Top Farms Cherry Butter is being recalled because it contains undeclared milk, which can pose a serious risk to consumers with milk allergies. The recall affects retail and food service packages.

    Product
    Rocky Top Farms Cherry Butter sold in 1 gallon food service and 10oz retail sizes. 10 oz retail units may be sold individually and as multi-pack and variety packs online.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0776-2021·2021-09-08

    Cyclobenzaprine Hydrochloride Tablets 7.5mg Recalled for Microbial Contamination

    Teva Pharmaceuticals USA is recalling Cyclobenzaprine Hydrochloride Tablets 7.5mg (4,992 bottles, batch 1408824A, expiration 08/2023) distributed nationwide due to out-of-specification microbial test results in an excipient ingredient.

    Product
    Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314, NDC 57237-266-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2378-2021·2021-09-08

    Baxter PrismaFlex Dialysis Tubing Sets Recalled Due to Sterilization Failure

    Baxter PrismaFlex dialysis tubing sets are being recalled because products labeled sterile may not have been properly sterilized due to sterilization contractor failures and data integrity issues.

    Product
    Baxter PrismaFlex, REF numbers: a) 106696 (M 60 SET) b) 106697 (M 100 SET) Expansion: c) 107144 (TPE2000 SET) d) 115307 (M 150 SET) e) 115309 (ST 100 SET) f) 955467 (M 150 SET) g) 955468 (ST 100 SET) h) 955595 (M 100 SET) i) 955596 (ST 150 SET) Used with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2357-2021·2021-09-08

    Medical Imaging Software Bug May Cause Incorrect X-ray Exposure

    Philips CombiDiagnost R90 imaging software has a bug where exposure settings may change unexpectedly, resulting in over or under-exposed X-ray images. About 66 systems in the US are affected.

    Product
    CombiDiagnost R90 Software Version R1.0 and R1.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2381-2021·2021-09-08

    COVID-19 Antibody Test Kit Recalled for Failing Validation Requirements

    Thera Test Laboratories is recalling 11 EL-Anti-SARS-CoV-2 IgM test kits distributed across six states because they failed to meet FDA's updated validation requirements for accurately detecting COVID-19 antibodies.

    Product
    EL-Anti-SARS-CoV-2 IgM Kit, Catalog #104-129, IVD. Submitted as EUA202129
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2385-2021·2021-09-08

    Diamondback 360 Gen2 Orbital Atherectomy System Crown Size Mislabeling Recall

    Cardiovascular Systems Inc. is recalling 8 units of the Diamondback 360 Gen2 Peripheral Orbital Atherectomy System due to potential mislabeling of crown sizes. Units packaged as 1.50mm Solid Crown may actually be 1.25mm Micro Crown and vice versa.

    Product
    DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.5MM SOLID, 145 CM, REF DBP-150SOLID145
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0958-2021·2021-09-08

    Hostess Soft White Hot Dog Buns Recalled for Listeria and Salmonella Risk

    Hostess Brands is recalling Soft White Hot Dog Buns due to positive environmental samples for Listeria and Salmonella found by the contract manufacturer. The product was distributed to retailers and distributors across 34 U.S. states.

    Product
    Hostess Soft White Hot Dog Buns, Net Wt. 12 OZ, UPC 888109110970
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-2389-2021·2021-09-08

    Marco Shoulder Stabilization Kit Recall Due to Sterilization Failure

    Aspen Surgical Products is recalling 4,270 Marco Shoulder Stabilization Kits manufactured between July 2019 and July 2021 due to bioburden levels exceeding sterilization validation limits, which may compromise sterile fields and increase infection risk.

    Product
    Marco Shoulder Stabilization Kit, Product Code 711100, (previous product code 100601), Sample Kit S711100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21C004000·2021-09-08

    Dorel Maxi-Cosi Pria 70 Child Seat Recall for Tether Anchor Defect

    Dorel Juvenile Group is recalling Maxi-Cosi Pria 70 convertible child seats because they may not adequately protect children from head injury in a crash if installed without a top tether.

    Product
    CHILD SEAT:VEHICLE TETHER ANCHOR recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2379-2021·2021-09-08

    Baxter Prismaflex Dialysis Membranes Recalled for Sterilization Failure

    Baxter is recalling Prismaflex HF 1000 dialysis membranes (Lot 20B2330M) because products labeled as sterile may not have been properly sterilized due to manufacturing defects and data manipulation. Non-sterile devices could pose infection risks to patients.

    Product
    Baxter prismaflex, HF 1000 PAES membrane, REF 107140 Used with Prismaflex or PrisMax control units for continuous fluid management and renal replacement therapies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V696000·2021-09-08

    Blue Bird Recalls 2022 Vision School Buses for Camera Obstruction

    Blue Bird is recalling 2022 Vision school buses because the collision mitigation camera may block the driver's view of the passenger side cross-view mirror, increasing pedestrian injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2384-2021·2021-09-08

    MY01 Continuous Compartmental Pressure Monitor Recalled for Out-of-Specification Needle

    MY01, INC. is recalling the MY01 Continuous Compartmental Pressure Monitor (37 units) due to an incorrect needle with out-of-specification trocar geometry. The affected devices may require higher force to penetrate patient skin.

    Product
    MY01 Continuous Compartmental Pressure Monitor, Reference Number MY01-0001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2382-2021·2021-09-08

    FDA Recalls COVID-19 Antibody Test Kits for Increased False Positive Risk

    Thera Test Laboratories is recalling EL-Anti-SARS-CoV-2 IgG kits due to cross-reactivity that may produce false positive results. The recalled lot numbers are 05204351 and 05204368, affecting distribution in six US states.

    Product
    EL-Anti-SARS-CoV-2 IgG Kit, Catalog #104-130. Submitted as EUA202128
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0903-2021·2021-09-08

    Strawberry Yogurt Granola Parfait Recalled for Undeclared Soy

    Loffredo Fresh Gardens Inc. is recalling Strawberry Yogurt Granola Parfait products sold under multiple brands because soy lecithin in the yogurt ingredient is not declared on the label, posing a risk to consumers with soy allergies.

    Product
    Strawberry Yogurt Granola Parfait packaged in clear plastic cups and labeled in the following ways: 1) Go Fresh Market Strawberry Granola Yogurt, Net wt. 6.5 oz (184 g), UPC 7 58870 32670 5, Distributed by Produce Innovation, Norwalk, IA; 2) HWY 28 Farms, Strawberry Yogurt…
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2383-2021·2021-09-08

    CoolSculpting Elite System Software Error May Misreport Thermal Events

    The CoolSculpting Elite System may incorrectly report or fail to report thermal events during treatment, potentially causing unnecessary re-treatment or continued use without awareness of a malfunction.

    Product
    CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
    Category
    Medical Device
    Distribution
    44 states