The Recall Desk

State

Ohio product recalls

72,907 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,719
Critical
2,106
Severe
2,413
Most recent
2026-09-09

Of the 11,719 recalls naming Ohio we have scored against our rubric, 2,106 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.

These figures cover only the 11,719 recalls whose distribution notice names Ohio specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1151–1175 of 84626

  • HighNHTSA·26V412000·2026-06-29

    Tiffin Motorhomes Recreational Vehicles Rooftop Fan Fire Risk Recall

    Tiffin Motorhomes is recalling certain 2026–2027 recreational vehicles with MaxxAir N-Series Maxxfan rooftop ventilation fans. The circuit board may overheat and increase the risk of fire.

    Product
    TIFFIN — TIFFIN ALLEGRO BREEZE, WAYFARER, ALLEGRO RED, BYWAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V411000·2026-06-29

    Jayco Recalls 2024 Alante and Vision RVs for Incorrect Weight Labels

    Jayco is recalling 2024 Alante and Entegra Vision recreational vehicles because the occupant and cargo capacity labels may list incorrect weights, potentially leading to vehicle overloading.

    Product
    JAYCO — JAYCO, ENTEGRA ALANTE, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V410000·2026-06-26

    Nissan Recalls 2025 Sentra Vehicles for Driveshaft Defect

    Nissan is recalling 2025 Sentra vehicles because a front left driveshaft may not be fully seated, risking transmission fluid leaks and loss of drive power.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V407000·2026-06-26

    Thomas Built School Bus Recall for Door Switch Failure

    Daimler Trucks is recalling 2026-2027 Thomas Built school buses because the entrance door may fail to open or close, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2, SAF-T-LINER EFX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V408000·2026-06-26

    Thomas Built Buses Recalls SAF-T-LINER HDX2 Due to Door Malfunction

    Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 buses because the entrance door may fail to open or close, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26577·2026-06-25

    MedPride baby oil lacks the required child-resistant packaging

    About 8,420 bottles of MedPride Baby Oil are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.

    Product
    MedPride Baby Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26578·2026-06-25

    Raychy children's light-up sneakers give children access to coin batteries

    About 500 pairs of Raychy Children's Light Sneakers are being recalled because the lithium coin batteries can be accessed easily by children, posing an ingestion hazard.

    Product
    Raychy Children's Light Sneakers Unisex
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26575·2026-06-25

    Super Off-Road solar power bank batteries can swell and overheat

    About 7,400 Super Off-Road 12,000 mAh Solar Wireless Power Banks are being recalled because the lithium-ion battery can swell and overheat, posing a burn hazard.

    Product
    Super Off-Road 12,000 mAh Solar Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26574·2026-06-25

    XW-A17 electric youth ATVs are missing required brake lights

    About 200 XW-A17 Electric Youth ATVs are being recalled because they are missing brake lights, violating the mandatory safety standard for ATVs.

    Product
    XW-A17 Electric Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26576·2026-06-25

    Lomi roll-on waxing kit power cords can overheat and short circuit

    About 14,700 Lomi Roll-On Waxing Kits are being recalled because the warmer's power cord can overheat and short circuit, posing fire, burn and shock hazards.

    Product
    Lomi Roll-On Waxing Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26580·2026-06-25

    Honlyne LED party favors give children access to button batteries

    About 13,400 sets of Honlyne LED party favors are being recalled because the battery compartments contain button cell batteries that can be easily accessed by children.

    Product
    Honlyne LED Party Favors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26581·2026-06-25

    Amana room air conditioners may stay energized during a ground fault

    About 13,514 Amana window and through-the-wall air conditioners and heat pumps are being recalled because the heating element can remain energized during a ground fault.

    Product
    Amana Window-Room-Air-Conditioners (WRAC) and Through the Wall (TTW) air conditioners or heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26582·2026-06-25

    Treatlife smoke and carbon monoxide detectors can fail to alarm

    About 20 Treatlife Smoke and Carbon Monoxide Detectors are being recalled because they can fail to alert consumers of a fire.

    Product
    Treatlife Smoke and Carbon Monoxide (CO) Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2396-2026·2026-06-24

    Arrow single lumen CVC kits contain drugs from recalled supplier

    Arrow central venous catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 35,540 units are affected.

    Product
    Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: 14 GA X 6 IN/CK-04711
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2385-2026·2026-06-24

    Arrow access trays and PSI kits contain recalled supplier drugs

    Arrow access trays and PSI kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 426,041 units are affected.

    Product
    Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH; PSI KIT: 9 FR X 10 CM/ASK-09903-PHP1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-UPA; PSI KIT: 9 FR X 4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2376-2026·2026-06-24

    Arrow central venous catheter kits contain drugs from a recalled supplier

    Arrow central venous catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 308,263 units affected.

    Product
    Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH; 3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH; MULT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2363-2026·2026-06-24

    Arrow paracentesis kits contain drugs from a recalled supplier

    Arrow paracentesis kits, REF AK-00376 and ASK-00376-VCU, are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 50,724 units affected.

    Product
    PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2365-2026·2026-06-24

    Arrow biopsy system comprehensive kits contain recalled supplier drugs

    Arrow Biopsy System Comprehensive Kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 14,840 units affected.

    Product
    Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2364-2026·2026-06-24

    Arrow access trays and StimuCath kits contain recalled supplier drugs

    Arrow access trays and StimuCath safety kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 205,685 units affected.

    Product
    Description/REF: ACCESS TRAY/ASK-04001-SUH-S; ACCESS TRAY/ASK-04001-VM1; STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS; STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS; STIMUCATH SFTY KIT: 20G CTH, 18Gx8CM NDL/AB-20608-KS; STIMUCATH KIT: 19G CATH, 17G x 9CM NDL/
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2387-2026·2026-06-24

    Arrow PI midline 5 Fr kits contain recalled supplier drugs

    The Arrow PI Midline two-lumen 5 Fr x 20 cm kit is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 90 units affected.

    Product
    Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2366-2026·2026-06-24

    Arrow pacing PSI kits contain drugs from a recalled supplier

    Arrow Pacing PSI kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 15,915 units are affected.

    Product
    Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, PACING PSI KIT: 5 FR 2L/ASK-07155-UPM
    Category
    Medical Device
    Distribution
    Distributed nationwide