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.

21076–21100 of 85144

  • HighCPSC·22233·2022-09-29

    Children's Bowtie Hairclips Recalled for Excessive Lead Content

    BE Jewel Accessories is recalling about 1,200 children's bowtie hairclips sold nationwide because the crystals exceed federal lead content limits. Lead poses a toxicity risk if ingested by young children.

    Product
    Children's Bowtie Hairclips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V724000·2022-09-29

    Chevrolet Equinox and GMC Terrain driver seat frame bolt defect

    General Motors is recalling certain 2022-2023 Chevrolet Equinox and 2022 GMC Terrain vehicles due to a potential issue with the driver's seat frame. The seat may not properly restrain an occupant in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V726000·2022-09-29

    Keystone Travel Trailers Recalled for Loose Hydraulic Leveling Foot Pads

    Keystone is recalling certain 2020-2023 travel trailers because hydraulic leveling leg foot pads may become loose and separate from the vehicle. A separated foot pad can become a road hazard, increasing the risk of a crash.

    Product
    KEYSTONE — KEYSTONE FUZION, ALPINE, IMPACT, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22237·2022-09-29

    HyperJuice 130W USB-C Battery Packs Recalled for Fire Hazard

    Hyper Products is recalling HyperJuice 130W USB-C Battery Packs because they can overheat while charging and pose a fire hazard. Two reports of overheating have resulted in smoke, melting, and property damage.

    Product
    HyperJuice 130W USB-C Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22781·2022-09-29

    Yamaha Viking Off-Road Side-by-Side Vehicles Recalled for Brake Hazards

    Yamaha is recalling about 330 Model Year 2022 Viking Off-Road Side-by-Side vehicles because improperly installed rear brake lines can leak brake fluid and reduce vehicle control, creating crash and injury hazards.

    Product
    Yamaha Viking Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22236·2022-09-29

    HyperJuice Stackable GaN USB-C Chargers Recalled for Fire Hazard

    Hyper Products is recalling about 18,200 HyperJuice Stackable GaN USB-C Chargers (models HJ414 65W and HJ417 100W) because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    HyperJuice Stackable GaN USB-C Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1748-2022·2022-09-28

    ANKUR Golden Raisins Recalled for Undeclared Sulfites

    ANKUR Golden Raisins (14 oz, UPC 8904 1740 10327) have been recalled due to undeclared sulfites. The voluntary recall affects 485 cases distributed to multiple states.

    Product
    ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case
    Category
    Food
    Distribution
    14 states
  • SevereNHTSA·22V722000·2022-09-28

    2023 Western Star 49X Trucks Recalled Due to Tie Rod Defects

    Certain 2023 Western Star and Freightliner trucks are being recalled because tie rod clamps may be improperly heat-treated and crack, potentially causing loss of steering control.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 6900, 4700, 4900, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1739-2022·2022-09-28

    Fifth Season Salad Kit Recalled for Undeclared Milk and Egg Allergens

    Fifth Season Crunchy Sesame Premium Salad Kit (6.1 oz, UPC 52070008147) is being recalled due to undeclared milk and egg allergens. Consumers with allergies or sensitivities to these ingredients should not consume this product.

    Product
    Fifth Season Crunchy Sesame Premium Salad Kit 6.1 oz (173g )UPC Code: 52070008147
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1758-2022·2022-09-28

    BD MaxGuard Extension Set Wrong Expiration Label Poses Infection Risk

    CAREFUSION is recalling 600 BD MaxGuard Extension Sets because labels list expiration year 2027 instead of 2025. Using expired products may cause leaks and infection risk.

    Product
    BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1753-2022·2022-09-28

    BD MaxGuard Extension Set Mislabeled With Wrong Expiration Date

    BD MaxGuard Extension Set units have labels listing 2027 as the expiration year instead of 2025. Using expired medical devices may compromise product integrity and increase the risk of leaks and infection.

    Product
    BD MaxGuard Extension Set, REF: ME1069
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1757-2022·2022-09-28

    BD MaxGuard Extension Sets Recalled for Mislabeled Expiration Dates

    CAREFUSION is recalling 17,250 BD MaxGuard Extension Set units with labels listing incorrect expiration year 2027 instead of 2025. Using expired products could compromise device integrity and create infection risk to patients and healthcare workers.

    Product
    BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1756-2022·2022-09-28

    BD MaxGuard Administration Set Recalled for Incorrect Expiration Date Labels

    BD MaxGuard Drop Administration set labels incorrectly list expiration year 2027 instead of 2025. Use of expired product risks compromised integrity, potential leaks, and patient or worker infection.

    Product
    BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1760-2022·2022-09-28

    BD MaxGuard Administration Set Recalled for Incorrect Expiration Labeling

    CAREFUSION is recalling BD MaxGuard 15 Drop Administration Sets with incorrect expiration year labels (showing 2027 instead of 2025). Use of expired product may compromise integrity and risk infection.

    Product
    BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1764-2022·2022-09-28

    FDA expands recall: HLS Set Advanced 7.0 sterility barrier compromise

    Maquet Medical Systems USA has expanded a recall for HLS Set Advanced 7.0, a preconnected medical device used for heart and lung support, due to a potential breach in the sterility barrier that could compromise product sterility.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1772-2022·2022-09-28

    Serological Test Positive Control Shows False Negative Results for Hepatitis B

    Randox Serology I Positive Control may test negative for Hepatitis B surface antigen (HBsAg) on certain analyzers despite being designed as a positive control, potentially affecting laboratory quality control procedures.

    Product
    The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2022·2022-09-28

    Hemodialysis Water Purification Unit Recalled for Missing EMI Shielding

    Fresenius is recalling 24 units of the AquaC UNO H reverse osmosis unit because internal ethernet cables lack ferrite cores, compromising electromagnetic compatibility in hemodialysis water purification systems.

    Product
    AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-10VA-1 Vivonic Part Number: G02000970-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1765-2022·2022-09-28

    Medical device set recalled for potential sterility barrier compromise

    Maquet Medical Systems USA is recalling the BEQ-HLS 5050 (HLS Set Advanced 5.0) due to a potential breach in the sterility barrier that may compromise product sterility.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1754-2022·2022-09-28

    BD MaxGuard Extension Set Mislabeled with Wrong Expiration Year

    BD MaxGuard Flow Controller Extension Set labels incorrectly list 2027 expiration instead of 2025. Use of expired product could compromise device integrity and create infection risk.

    Product
    BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1759-2022·2022-09-28

    BD MaxGuard Extension Set Recalled for Incorrect Expiration Year

    CAREFUSION's BD MaxGuard Extension Set is being recalled because product labels incorrectly list expiration year 2027 instead of 2025. Using expired product may compromise integrity, potentially causing leaks and infection risk.

    Product
    BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171
    Category
    Medical Device
    Distribution
    39 states
  • HighNHTSA·22V721000·2022-09-28

    Rolls-Royce Phantom Headlight Coating Defect Recall

    BMW is recalling 2023 Rolls-Royce Phantom vehicles because headlights may lack metal coating, causing low beams to fail FMVSS 108 and increasing crash risk.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE PHANTOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1752-2022·2022-09-28

    BD MaxGuard Extension Set labeled with incorrect expiration year 2027

    46,900 BD MaxGuard Extension Sets are labeled with expiration year 2027 but should expire in 2025. Using expired product may compromise integrity and cause leaks, risking infection.

    Product
    BD MaxGuard Extension Set with 4-way stopcock, REF: M4058
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-1776-2022·2022-09-28

    FDA Recalls Grappler Suture Anchors Due to Potential Breakage Risk

    Paragon 28, Inc. is recalling Grappler Suture Anchors (REF: P44-110-3010-SK, Lot 5007499) due to risk that the anchor may break upon insertion, potentially leaving debris in patients and delaying surgery.

    Product
    Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1767-2022·2022-09-28

    Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach

    Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1755-2022·2022-09-28

    BD MaxGuard Flow Controller Extension Set recalled for mislabeled expiration dates

    CAREFUSION is recalling BD MaxGuard Flow Controller Extension Sets because product labels show expiration year 2027 instead of 2025. Using expired sets risks product integrity failure and potential patient infection.

    Product
    BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141
    Category
    Medical Device
    Distribution
    39 states