The Recall Desk

State

Iowa product recalls

73,388 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,590
Critical
910
Severe
1,590
Most recent
2026-09-30

Of the 5,590 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 5,590 recalls whose distribution notice names Iowa specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20776–20800 of 78978

  • ModerateFDA (Drugs)·D-1306-2022·2022-08-17

    Glenmark Pharmaceuticals Recalls Telmisartan/Hydrochlorothiazide Due to Defective Blister Packs

    Glenmark Pharmaceuticals Inc., USA is recalling specific lots of Telmisartan and Hydrochlorothiazide tablets due to complaints of defective blister packs that are difficult to open and cause tablets to break during removal.

    Product
    TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1329-2022·2022-08-17

    Lamotrigine Tablets Recalled for Label Strength Error

    AVKARE Inc. is recalling 8,328 bottles of Lamotrigine Tablets, USP 100 mg nationwide due to a labeling error in the declared strength.

    Product
    LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1314-2022·2022-08-17

    FDA Recalls SYSTANE Lubricant Eye Drops Due to Improper Storage

    McKesson Medical-Surgical Inc. is recalling 47 bottles of SYSTANE Lubricant Eye Drops nationwide. The products were stored outside label specifications, violating manufacturing practices.

    Product
    SYSTANE LUBRICANT — SYSTANE LUBRICANT (POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1316-2022·2022-08-17

    Eye Drops Recalled for Improper Storage Outside Specifications

    SYSTANE BALANCE lubricant eye drops (12 boxes, nationwide) are being recalled because they were stored outside the manufacturer's label specifications. The FDA classified this as a Class II recall.

    Product
    SYSTANE BALANCE — SYSTANE BALANCE (PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1321-2022·2022-08-17

    FDA Recalls Pataday Eye Allergy Drops Due to Storage Deviations

    Mckesson Medical-Surgical is recalling Pataday Once Daily Relief eye drops nationwide because the products were stored outside label specifications. No illnesses have been reported.

    Product
    PATADAY ONCE DAILY RELIEF — PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1312-2022·2022-08-17

    Bisacodyl suppositories recalled nationwide due to improper storage

    McKesson Medical-Surgical is recalling Bisacodyl suppositories stored outside label specifications. The FDA Class II recall affects 45 boxes distributed nationwide.

    Product
    BISACODYL — BISACODYL (BISACODYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1324-2022·2022-08-17

    Asthmanefrin Racephinephrine Inhalation Solution Recalled Due to Improper Storage

    Asthmanefrin Racephinephrine Inhalation Solution is being recalled because batches were stored outside the conditions specified on the drug label. The recall affects products distributed nationwide.

    Product
    Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1305-2022·2022-08-17

    Prescription Drug Recall: Telmisartan-Hydrochlorothiazide Tablets Due to Defective Packaging

    Glenmark Pharmaceuticals recalls 72,288 units of Telmisartan-Hydrochlorothiazide 80/25 mg tablets nationwide due to defective blister packaging that is difficult to open and causes tablets to break.

    Product
    TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2022·2022-08-17

    FDA Recalls Dakin's Solution Due to Storage Condition Deviations

    McKesson Medical-Surgical recalled 113 bottles of Dakin's Solution (sodium hypochlorite) nationwide due to improper storage outside label specifications. Products may have compromised stability.

    Product
    DAKINS QUARTER — DAKINS QUARTER (SODIUM HYPOCHLORITE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1318-2022·2022-08-17

    Earwax Removal Aid Debrox Recalled Nationwide for Improper Storage Conditions

    Debrox earwax removal aid is recalled nationwide because 131 boxes of the product were stored outside label-specified conditions. Consumers should discontinue use and consult a healthcare provider if needed.

    Product
    DEBROX — DEBROX (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1322-2022·2022-08-17

    FDA Recalls A&D Original Ointment due to improper storage conditions

    A&D Original Ointment 16 oz jars are being recalled nationwide because products were stored outside manufacturer specifications. The recall affects all NDC 11523-0096-3 units distributed in the USA.

    Product
    A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1325-2022·2022-08-17

    Racepinephrine Inhalation Solution Recalled for Improper Storage Conditions

    Mckesson Medical-Surgical is recalling S2 Racepinephrine Inhalation Solution due to storage that deviated from label specifications. This Class II recall affects 23 cartons distributed nationwide.

    Product
    S2 — S2 (RACEPINEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V628000·2022-08-16

    Man Cave RV Recalls Toy Haulers Due to Gas Leak Risk

    Man Cave RV is recalling 2018-2020 Toy Haulers because an overtightened saddle valve bolt may damage the o-ring seal, causing a continuous gas leak that increases fire risk.

    Product
    MAN CAVE — MAN CAVE TOY HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22200·2022-08-15

    4moms MamaRoo and RockaRoo Baby Swings and Rockers Strangulation Hazard

    4moms is recalling over 2 million MamaRoo baby swings and 220,000 RockaRoo rockers because dangling restraint straps pose a strangulation hazard to crawling infants. One death has been reported.

    Product
    4moms MamaRoo Baby Swing, versions 1.0 through 4.0 and RockaRoo Baby Rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V625000·2022-08-15

    Spartan Fire Recalls One 2022 MetroStar Fire Truck for Engine Defect

    Spartan Fire is recalling one 2022 MetroStar fire truck because the engine control module may short-circuit, causing an unexpected engine shutdown that increases crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V627000·2022-08-15

    2020-2021 Hyundai Palisade windshield wiper motor failure recall

    Hyundai is recalling certain 2020-2021 Palisade vehicles due to windshield wiper motor failure. The inoperative wipers reduce visibility and increase crash risk.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V626000·2022-08-15

    2020-2022 Kia Telluride tow hitch electrical short fire hazard

    Certain 2020-2022 Kia Telluride vehicles with Genuine Kia tow hitch harnesses may experience electrical shorts from debris and moisture, creating a fire risk while parked or driving.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V622000·2022-08-12

    Seagrave Recalls 2022 Marauder Fire Trucks Due to Steering Gear Defect

    Seagrave is recalling 2022 Marauder fire trucks because incorrectly assembled steering gears may fracture, potentially causing a loss of steering control and increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V623000·2022-08-12

    Ford Recalls 2021-2022 F-150 Trucks for Driveshaft Fracture Risk

    Ford is recalling 2021-2022 F-150 vehicles because underbody insulators may loosen and damage the driveshaft, potentially causing loss of vehicle control.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide