The Recall Desk

State

Iowa product recalls

73,509 recalls have nationwide distribution and so reach Iowa. 5,592 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,592
Critical
910
Severe
1,590
Most recent
2026-10-14

Of the 5,592 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 1,590 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,592 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.

24351–24375 of 79101

  • ModerateFDA (Drugs)·D-0270-2022·2021-12-15

    Fexofenadine and Pseudoephedrine Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended Release Tablets because they failed dissolution specifications, which may affect how the medication works in the body.

    Product
    Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 20 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0271-2022·2021-12-15

    Antihistamine and Decongestant Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets distributed by Rugby Laboratories due to failed dissolution specifications. Affected lot AC2103329D (Exp 1/2023) was distributed nationwide in 2,184 cartons.

    Product
    Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 30 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0274-2022·2021-12-15

    Walmart Allergy Relief D Extended-Release Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Walmart brand Allergy Relief D extended-release tablets (Lot #AC2103329B) nationwide because the tablets failed to meet dissolution specifications, which may affect medication effectiveness.

    Product
    Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0276-2022·2021-12-15

    Hydrocodone Bitartrate and Acetaminophen tablets recalled for product mix-up

    Ascent Pharmaceuticals is recalling Hydrocodone Bitartrate and Acetaminophen 10 mg/325 mg tablets nationwide due to a product mix-up. The recall affects 9,744 bottles and was voluntarily initiated by the manufacturer.

    Product
    HYDROCODONE BITARTRATE AND ACETAMINOPHEN — HYDROCODONE BITARTRATE AND ACETAMINOPHEN (HYDROCODONE BITARTRATE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0273-2022·2021-12-15

    CVS Allergy Relief D Extended-Release Tablets Recall

    CVS Allergy Relief D extended-release tablets (Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg) are being recalled because they failed dissolution specifications, meaning the tablets may not release the medication properly.

    Product
    Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, 30 Extended-Release Tablets USP, Distributed By CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI 02985, Made in India, NDC 69842-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0275-2022·2021-12-15

    Fexofenadine and Pseudoephedrine Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets because they failed to meet dissolution specifications, which may affect how the medication works in the body.

    Product
    FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0268-2022·2021-12-15

    CVS Allergy & Congestion Relief Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling CVS Allergy & Congestion Relief tablets (fexofenadine HCl 60 mg/pseudoephedrine HCl 120 mg extended-release) nationwide due to failed dissolution specifications.

    Product
    Allergy & Congestion Relief Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets, 20 extended-release tablets, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Made in India, NDC 69842-249-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0272-2022·2021-12-15

    Fexofenadine and Pseudoephedrine allergy relief tablets recalled for failed dissolution

    Dr. Reddy's Laboratories is recalling a 12 HR Allergy & Congestion Relief product distributed nationwide because the tablets failed to meet dissolution specifications, which may affect drug effectiveness.

    Product
    12 HR Allergy & Congestion Relief Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg Antihistamine I Nasal Decongestant, 20 Extended-Release Tablets USP, Distributed By Cardinal Health, Dublin, Ohio 43107, Made in India, NDC 70000-0518-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·047-2021·2021-12-14

    Margherita Pepperoni Recalled for Possible Bacillus Cereus Contamination

    Smithfield Packaged Meats is recalling approximately 10,990 pounds of Margherita pepperoni due to possible Bacillus cereus contamination. No illnesses have been reported.

    Product
    Smithfield Packaged Meats Corp. Dba Margherita Meats Inc. Recalls Pepperoni Products Due to Possible Bacillus Cereus Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V969000·2021-12-14

    Spartan K3 RV Chassis Models Recalled for Fuel System Defect

    Shyft Group is recalling 2020-2023 Spartan K3 RV chassis vehicles because fuel tubes may fatigue and crack, creating a potential fuel leak and fire risk. Dealers will install vibration isolators or replace fuel tubes at no cost.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V961000·2021-12-13

    Mercedes-Benz Recalls Vehicles Due to Fuel Leak Fire Risk

    Mercedes-Benz is recalling specific gasoline-engine vehicles because trapped particles may cause a fuel leak, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63, GLB 250, AMG A35, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V962000·2021-12-13

    Sutphen Recalls 2016-2020 Fire Trucks Due to Fuel Leak Risk

    Sutphen is recalling 2016-2020 fire trucks because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    SUTPHEN — SUTPHEN FIRE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V963000·2021-12-13

    2022 Toyota 4Runner recalled for inoperable high beam after fog light installation

    Southeast Toyota Distributors is recalling certain 2022 Toyota 4Runner vehicles because the driver's side high beam may become inoperable after installation of accessory fog lights. This reduces visibility and increases crash risk.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V966000·2021-12-13

    Autocar Xpeditor GPS Module Mounting Defect May Interfere With Brakes

    Autocar is recalling certain 2021-2022 Xpeditor vehicles because the GPS module may be improperly mounted and could come loose, potentially interfering with brake and throttle pedals.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V965000·2021-12-13

    Western Star and Freightliner Trucks Fuel Tubes May Crack, Fire Risk

    Fuel tubes in certain 2019–2022 Western Star, Freightliner, and FCCC trucks may crack, causing high-pressure fuel leaks that could ignite. DTNA is offering free replacement of fuel tubes and installation of vibration isolators.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 4700, 114SD, 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V964000·2021-12-13

    Seagrave Fire Trucks Recalled for Fuel Tube Cracking and Fire Risk

    Seagrave is recalling 2019-2021 fire trucks with Cummins X12 engines because fuel tubes may crack, causing high-pressure leaks and fire risks.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, ATTACKER, MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V960000·2021-12-10

    KME Predator Fire Risk Recall Due to Fuel Tube Cracking

    KME is recalling 2020-2022 Predator and Severe Service vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    KME — KME PREDATOR SS, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22029·2021-12-10

    Target Recalls Decorative Mailbox Due to Laceration Hazard

    Target is recalling approximately 174,300 Letters to Santa Mailboxes because the mail slot can be sharp, posing a laceration hazard. Target has received seven reports of lacerations, three of which required medical attention.

    Product
    Letters to Santa Mailbox
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V954000·2021-12-09

    Subaru Recalls 2020 Ascent Vehicles for Steering Tie Rod Defect

    Subaru is recalling 2020 Ascent vehicles because front tie rod ends may not fit properly, potentially causing loss of steering control and increasing crash risk.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide