The Recall Desk

State

Ohio product recalls

73,388 recalls have nationwide distribution and so reach Ohio. 11,756 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,756
Critical
2,117
Severe
2,903
Most recent
2026-10-07

Of the 11,756 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,903 (25%) are Severe.

These figures cover only the 11,756 recalls whose distribution notice names Ohio specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21426–21450 of 85144

  • ModerateFDA (Devices)·Z-1668-2022·2022-09-07

    DeRoyal Sterile Custom Kits Recalled for Defective Connectors

    DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors are being recalled because the procedure packs contained a recalled product. Approximately 1,306 kits were distributed in Ohio and Tennessee.

    Product
    DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1471-2022·2022-09-07

    Timolol Maleate eye drops recalled for unknown impurity in stability testing

    Akorn, Inc. is recalling Timolol Maleate Ophthalmic Solution due to identification of an unknown impurity during 12-month stability testing. No illnesses have been reported.

    Product
    Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-189-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1467-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions

    Colgate Anticavity Fluoride Toothpaste OPTIC WHITE ADVANCED ICY FRESH is recalled due to improper temperature storage during manufacturing. Approximately 1,680 packages distributed across 11 U.S. states are affected.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY FRESH, Net Wt. 3.2 OZ. (90 g) UPC 0 35000 97159 3. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1472-2022·2022-09-07

    Nighttime Sleep-Aid tablets recalled due to carton labeling error

    CVS Pharmacy is recalling Nighttime Sleep-Aid tablets because the carton incorrectly identifies the active ingredient as doxylamine succinate HCl instead of doxylamine succinate. Approximately 257,064 cartons were distributed nationwide.

    Product
    Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 34873 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1678-2022·2022-09-07

    Frozen Lentil Soup Recalled for Undeclared Wheat Allergen

    Yem Foods LLC is recalling Priyems Sambar Spicy Lentil Soup for containing undeclared wheat starch in an ingredient. Consumers with wheat allergies should not consume this product.

    Product
    Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-1680-2022·2022-09-07

    Lemon Pickle Recalled Due to Undeclared Wheat Starch Allergen

    Yem Foods LLC is recalling Priyems Lemon Pickle due to undeclared wheat starch found in asafoetida, a spice ingredient. Consumers with wheat allergies or celiac disease should not consume affected products.

    Product
    Priyems Lemon Pickle 1lb/454g UPC 8 61754 000117, 10 retail units per wholesale case, Refrigerated
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-1497-2022·2022-09-07

    Triamcinolone Acetonide Cream Recalled for Manufacturing Defects

    Padagis US LLC is recalling 57,816 tubes of Triamcinolone Acetonide Cream 0.1% nationwide due to manufacturing process deviations. Consumers reported gritty texture and reduced effectiveness.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1646-2022·2022-09-07

    X-ray imaging system hardware defect may prevent operation

    Siemens is recalling certain X-ray imaging systems due to a potential hardware issue with the error detection mechanism. In rare cases, this could prevent X-ray emission until system shutdown.

    Product
    Artis pheno- Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1469-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled Due to Improper Storage Conditions

    Family Dollar Stores recalls 1,400 packages of Colgate Anticavity Fluoride Toothpaste due to improper temperature storage conditions during manufacturing. The product may not meet quality standards.

    Product
    Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT PASTE. Net Wt. 4.2 OZ. (119 g) UPC 0 35000 45836 0. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2022·2022-09-06

    Magnolia Provision Company recalls beef jerky products due to possible Listeria contamination

    Magnolia Provision Company, Inc. is recalling beef jerky products because laboratory testing detected possible Listeria monocytogenes contamination.

    Product
    Magnolia Provision Co., Inc. — Magnolia Provision Company, Inc., Recalls Beef Jerky Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V669000·2022-09-06

    Alamo Group Recalls All JetVac Vehicles Due to Hose Reel Defect

    Alamo Group is recalling 2019-2022 All JetVac vehicles because a short clevis can cause the hose reel to fall, increasing injury risk.

    Product
    ALAMO GROUP — ALAMO GROUP ALLJETVAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V663000·2022-09-01

    Jayco and Entegra motorhomes recalled for suspension torsion bar defect

    Entegra and Jayco motorhomes may have incorrectly installed torsion bar shims causing potential suspension failure. Dealers will replace the defective component free of charge.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE, MELBOURNE PRESTIGE, QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V664000·2022-09-01

    Vermeer Recalls Vac-Tron Vacuum Excavator Trailers Due to Frame Defect

    Vermeer is recalling specific Vac-Tron vacuum excavator trailers because the frame may bend or distort, potentially causing loss of stability and control while towing.

    Product
    VAC-TRON — VAC-TRON AIR555SDT, AIR855SDT, AIR753SDT, AIR833SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V662000·2022-09-01

    Honda CRF1100 Africa Twin Motorcycles Recalled for Engine Control Software Bug

    Honda is recalling 2020-2021 CRF1100 Africa Twin motorcycles due to an ECU software error that may cause engine stall or loss of drive power. Owners can get a free software update from dealers.

    Product
    HONDA — HONDA CRF1100 AFRICA TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22215·2022-09-01

    UPPAbaby RIDGE Jogging Strollers Recalled for Fingertip Amputation Hazard

    UPPAbaby is recalling about 14,400 All-Terrain RIDGE jogging strollers because openings in the rear disc brakes can catch and amputate a child's fingertip. One injury has been reported.

    Product
    UPPAbaby All-Terrain RIDGE Jogging Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V666000·2022-09-01

    2021-2022 Nissan Rogue Rear Seat Belts May Fail to Retract

    Nissan is recalling certain 2021-2022 Rogue vehicles where rear seat belts may not retract properly, making them difficult to use. This could prevent proper seatbelt usage in a crash. Dealers will replace affected seat belts for free.

    Product
    NISSAN — NISSAN ROGUE, redundant ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V665000·2022-09-01

    Motorhome recall: missing engine air intake drain increases crash risk

    Jayco is recalling 2021-2023 Entegra and Jayco motorhomes for a missing water drain in the engine air intake box. Water can accumulate and enter the engine, causing engine failure and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO REATTA, CORNERSTONE, ASPIRE, EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22768·2022-09-01

    Yuboloo Infant Bath Seats Recalled for Drowning Hazard

    Yuboloo is recalling about 1,050 infant bath seats sold on Amazon.com from May to November 2021 because they fail to meet federal safety standards and can tip over in water, posing a drowning hazard to infants.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22769·2022-09-01

    Otter MOMO Children's Sandals Recalled for Excess Lead Content

    Kolan LLC is recalling about 100 Otter MOMO children's sandals sold on Amazon.com from March through April 2022 because the inner layer exceeds federal lead content limits. Lead can be toxic if ingested by young children.

    Product
    Otter MOMO Children's Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V661000·2022-09-01

    2022 Lexus NX and Toyota Tundra Electronic Parking Brake Failure

    Certain 2022 Lexus NX and Toyota Tundra vehicles' electronic parking brake systems may fail to engage because the Skid Control ECU falsely detects an overcurrent condition. This increases the risk of vehicle rollaway.

    Product
    LEXUS — LEXUS, TOYOTA NX350, TUNDRA, NX250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22214·2022-09-01

    TJX Recalls Novogratz Outdoor Metal Hanging Chairs Due to Fall Hazard

    TJX Companies is recalling about 5,000 Novogratz outdoor metal hanging chairs sold nationwide. These chairs can tip or fall while occupied, or the supporting hooks or chains can break, causing 16 reported injuries including bruises and a mild concussion.

    Product
    Novogratz brand Outdoor Metal Hanging Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22213·2022-09-01

    Sun Joe Cordless Lawn Mowers Recalled for Blade Detachment Risk

    Snow Joe is recalling approximately 26,300 Sun Joe cordless lawn mowers (models 24V-X2-17LM and 24V-X2-17LM-CT) because the mower blade can detach unexpectedly, posing a laceration hazard.

    Product
    Sun Joe Cordless Lawn Mowers models 24V-X2-17LM and 24V-X2-17LM-CT
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1522-2022·2022-08-31

    INTERA 3000 implantable pump recalled for higher-than-expected flow rate

    The FDA is recalling INTERA 3000 implantable hepatic infusion pumps due to a malfunction causing higher-than-expected medication flow rates. Patients should contact their healthcare provider.

    Product
    INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
    Category
    Medical Device
    Distribution
    13 states