The Recall Desk

State

Kentucky product recalls

73,388 recalls have nationwide distribution and so reach Kentucky. 7,197 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,197
Critical
1,409
Severe
2,024
Most recent
2026-10-07

Of the 7,197 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,024 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,197 recalls whose distribution notice names Kentucky specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20926–20950 of 80585

  • 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 (Devices)·Z-1508-2022·2022-08-17

    Cholestech LDX cholesterol test cassettes require bilirubin interference label update

    Alere is updating the package insert for Cholestech LDX cholesterol test cassettes to disclose that samples with elevated bilirubin can produce inaccurate triglyceride and HDL results. Approximately 436,990 units are affected.

    Product
    The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL cholesterol, triglycerides and glucose. Samples used for testing can be whole blood from a fingerstick (collected in a lithium heparin-coated capillary tube)…
    Category
    Medical Device
    Distribution
    31 states
  • 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
  • SevereCPSC·22199·2022-08-11

    Residential Elevators recalled for child entrapment hazard

    Residential Elevators, Inc. is recalling about 31,000 home elevators sold since 1986 because young children can become trapped between the exterior and interior doors, risking serious injury or death.

    Product
    Residential Elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V619000·2022-08-11

    2022 Chrysler Pacifica windshield wipers may not function due to loose arm nuts

    Certain 2022 Chrysler Pacifica and Voyager vehicles have improperly tightened windshield wiper arm nuts, causing malfunction. This reduces driver visibility and increases crash risk. Dealers will tighten the nuts free of charge.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V620000·2022-08-11

    Rosenbauer Fire Trucks Recalled for Engine Control Module Short-Circuit Risk

    Rosenbauer America is recalling 2022 Commander and 2023 Commercial M2-106 fire trucks because an engine control module short-circuit may cause unexpected engine shutdown.

    Product
    ROSENBAUER — ROSENBAUER COMMERCIAL M2-106, COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V618000·2022-08-11

    2023 Grand Design Momentum fifth wheels ramp door fall hazard

    Grand Design is recalling 2023 and 2022 Momentum fifth wheels due to a defective ramp door cut-off switch that may allow the electric ramp door to fall, creating an injury risk.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22766·2022-08-11

    Footpads for Onewheel GT Electric Skateboards Recalled for Injury Hazard

    Future Motion is recalling front footpads for Onewheel GT electric skateboards because the footpad can fail to disengage after the rider dismounts, causing the skateboard to continue operating and potentially injure bystanders.

    Product
    Footpads for Onewheel GT Electric Skateboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V617000·2022-08-11

    Third-Row Seat Belt Buckle Rivet Defect in 2021-2022 GMC Yukon and Related Vehicles

    General Motors is recalling 484,155 vehicles with improperly formed rivets on third-row seat belt buckle assemblies. The defect may prevent proper seat belt restraint in a crash, increasing injury risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide