The Recall Desk

State

Iowa product recalls

73,104 recalls have nationwide distribution and so reach Iowa. 5,588 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,588
Critical
910
Severe
1,319
Most recent
2026-09-23

Of the 5,588 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 1,319 (24%) are Severe.

These figures cover only the 5,588 recalls whose distribution notice names Iowa specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11151–11175 of 78692

  • ModerateFDA (Devices)·Z-2245-2024·2024-07-10

    Medical Device Calibrator Kit Assigned Extended Incorrect Expiration Date

    Ortho-Clinical Diagnostics is recalling a calibrator kit with an incorrect expiration date that could bias lab results if used past its true expiration date.

    Product
    VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate the VITROS 5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems for the quantitative measurement of total iron-binding capacity (TIBC) using VITROS Chemistry Products dTIBC Reagent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0573-2024·2024-07-10

    Drug Recall: Little Moon Essentials Aching Head Rub for Manufacturing Defects

    Little Moon Essentials Aching Head Rub is being recalled by the manufacturer for manufacturing deviations. The voluntary recall affects 6,312 units distributed nationwide and in Ontario, Canada.

    Product
    Little Moon Essentials, Aching Head Rub (Camphor 3.09%, Menthol 2.55%) , a) 0.5OZ (14G), metal tin, UPC Code 67367388226 8, NDC 70722-203-05; b)1OZ (28G) glass jar, UPC Code 6 73673 88203 9, NDC 70722-203-01; Little Moon Essentials LLC Dania Beach, Fl 33004
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0584-2024·2024-07-10

    Venlafaxine Extended-Release Capsules Recalled for Failed Dissolution

    The FDA is recalling Venlafaxine Hydrochloride extended-release capsules (37.5mg) distributed nationwide because routine stability testing revealed the capsules failed to meet dissolution specifications, potentially affecting drug effectiveness.

    Product
    Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton, Rx only, Mfg by: Cadila Healthcare Ltd., Ahmedabad, India, Distributed by: Major Pharmaceutical 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, USA, NDC 0904-7075-61…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0572-2024·2024-07-10

    Topical Pain-Relief Product Recalled Due to Manufacturing Violations

    Little Moon Essentials Crampy Belly Rub, a camphor-based topical product, is being recalled nationwide and in Canada due to manufacturing deviations. The firm-initiated recall affects 788 glass jars.

    Product
    Little Moon Essentials, Crampy Belly Rub (Camphor 1.1%), Packaged as a) 4 FL OZ (118ML) glass jar, UPC Code 6 73673 88260 2, NDC 70722-260-04; b) 2 FL OZ (59ML) glass jar, UPC Code 6 73673 88204 6, NDC 70722-260-02, Little Moon Essentials LLC Dania Beach, Fl 33004
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0580-2024·2024-07-10

    Dodex Injectable Cyanocobalamin Recalled Due to Subpotent Drug Defect

    Accord Healthcare is recalling Dodex Injectable (Cyanocobalamin) due to subpotency; affected batches contain less active ingredient than labeled. Patients using affected lots should contact their healthcare provider.

    Product
    Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad-382 210, India, NDC 16729-533-08, UPC Code: 031672953308
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1459-2024·2024-07-10

    Botanical Herbal Supplement Recalled for Potential Yeast and Mold Contamination

    Grato Holdings is recalling BioActive Nutritional MINAPLEX botanical herbal supplement due to potential yeast and mold contamination. The recall involves 261 bottles (lot J28761) distributed nationwide in the US and Canada.

    Product
    BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml) bottle.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0577-2024·2024-07-10

    Little Moon Essentials Asana Kisser Drug Recalled Due to CGMP Deviations

    Little Moon Essentials Asana Kisser, a topical product containing camphor and menthol, is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects 320 units distributed in the United States and Canada.

    Product
    Little Moon Essentials, Asana Kisser, (Camphor 1.35%, Menthol 2.86%), Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 88227 5, NDC 70722-216-05; b) 3 OZ (85-05G) metal tin UPC Code 6 73673 88216 9, NDC 70722-216-03; Little Moon Essentials LLC Dania Beach, Fl 33004
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2260-2024·2024-07-10

    Stryker Curved Cement Delivery Needles Recalled: Expired Products Distributed

    Stryker recalled its Curved Cement Delivery Needle (Lot 6659783) due to expired product distribution. Three units were distributed to customers in Arkansas, California, Colorado, Florida, and Michigan.

    Product
    Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the ability to inject bone cement into multiple different areas through a single point…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0571-2024·2024-07-10

    Drug Recall: Little Moon Essentials Magical Muscle Oil due to CGMP Deviations

    Little Moon Essentials is recalling Magical Muscle Oil due to manufacturing practice deviations. The recall affects 1,654 glass jars distributed nationwide in the USA and Canada.

    Product
    Little Moon Essentials, Magical Muscle Oil, (Camphor 1.95%, Menthol 3.75%) packaged as: a) 2 FL OZ (59ML) glass jar, UPC Code 6 73673 88202 2, NDC 70722-246-02; b) 4 FL OZ (118ML) jar, UPC Code 6 73673 88233 6, NDC 70722-246-04; Little Moon Essentials LLC Dania Beach, Fl 33004
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E059000·2024-07-09

    JecoEV Tesla to CCS Charging Adapter Recall for Fire and Shock Risk

    Dongguan Biaoming is recalling JecoEV Tesla to CCS charging adapters sold on Amazon due to missing over-temperature protection and insecure latching, posing fire and electrical shock risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V517000·2024-07-09

    2023 to 2024 Mercedes-Benz Sprinter Rear Suspension U-Bolt Recall

    Daimler Vans USA is recalling certain 2023-2024 Mercedes-Benz Sprinter vehicles due to rear suspension U-bolts with reduced strength from improper heat-treatment. The defect can cause the rear axle to shift, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V523000·2024-07-09

    Prevost buses recalled for defective wheelchair lift bridging device

    Prevost recalls certain 2005-2024 buses with wheelchair lifts due to a potentially steep bridging device that can cause wheelchair instability. Affected owners should contact Prevost for a free replacement.

    Product
    PREVOST — PREVOST H3-41, X3-45, H3-45, H3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V524000·2024-07-09

    Volvo Bus 9700 Recall for Steering Gear Link Rod Nut Tightening

    Volvo Bus is recalling 2024 9700 vehicles because improperly tightened nuts on the steering gear link rod may loosen, potentially causing loss of steering control.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V518000·2024-07-08

    2021-2024 Nova Bus LFS Parking Brake Air Leak Recall

    Nova Bus is recalling 2021-2024 LFS buses due to an air leak in the parking brake valve that can cause unexpected parking brake engagement without activating brake lights, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V515000·2024-07-08

    Autocar Recalls 2023-2024 Xpeditor Trucks for Cab Tilt Hinge Pin Defect

    Autocar is recalling 841 2023-2024 Xpeditor trucks because a missing retaining ring on the cab tilt hinge pin could cause the pin to separate, creating a road hazard and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V519000·2024-07-08

    Nova Bus LFS windshield wiper blade alignment defect recall

    Nova Bus is recalling certain 2022-2023 LFS buses due to incorrectly aligned windshield wiper arms that can cause wiper blades to collide. Damaged blades reduce visibility and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V516000·2024-07-08

    2021-2022 Jeep Cherokee Curtain Airbag Connector May Fail to Deploy

    Chrysler is recalling 2021-2022 Jeep Cherokee vehicles with improperly secured right-side curtain airbag connectors that may prevent deployment, increasing injury risk in a crash.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2024·2024-07-05

    Al-Safa Recalls Frozen Chicken Products Due to Listeria Contamination

    Al-Safa US LLC is recalling approximately 2,010 pounds of frozen ready-to-eat chicken products that may be contaminated with Listeria monocytogenes.

    Product
    Al-Safa US LLC Recalls Frozen Ready-To-Eat Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2140-2024·2024-07-03

    Life2000 Ventilator systems recalled due to battery charging failure risk

    The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.

    Product
    Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.
    Category
    Medical Device
    Distribution
    Distributed nationwide