The Recall Desk

State

South Carolina product recalls

73,381 recalls have nationwide distribution and so reach South Carolina. 7,145 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,145
Critical
1,278
Severe
2,166
Most recent
2026-09-23

Of the 7,145 recalls naming South Carolina we have scored against our rubric, 1,278 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,166 (30%) are Severe.

Which agencies issued them

These figures cover only the 7,145 recalls whose distribution notice names South Carolina specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19576–19600 of 80526

  • SevereUSDA FSIS·044-2022·2022-12-15

    Mountain View Packaging Recalls Frozen Crispy Chicken Entrée for Undeclared Shrimp

    Mountain View Packaging is recalling frozen Crispy Chicken with Almonds entrée due to undeclared shrimp, a known allergen. No adverse reactions have been reported.

    Product
    Mountain View Packaging, LLC — Mountain View Packaging, LLC, Recalls Frozen Ready-To-Eat Crispy Chicken with Almonds Entrée Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23716·2022-12-15

    Gyroor C3 E-Bikes Recalled for Fire and Burn Hazards

    Gyroor C3 e-bikes are recalled because the battery pack can ignite, creating fire and burn hazards. Gyroor has received reports of battery packs igniting and injuries requiring medical treatment, including burns and smoke inhalation.

    Product
    Gyroor C3 e-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V930000·2022-12-15

    Chevrolet Bolt EV Pretensioner Exhaust Fire Risk Recall

    General Motors recalls 2017-2023 Chevrolet Bolt EV vehicles. After a crash with pretensioner deployment, pretensioner exhaust may ignite carpet near the B-pillar, creating a fire hazard.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E100000·2022-12-15

    Ridewell 266 Suspension Brake Pad Retaining Clip Recall

    Ridewell is recalling certain 266 Suspensions with Haldex Air Disc Brakes because a retaining clip may detach, reducing brake performance or causing a flat tire.

    Product
    SERVICE BRAKES, AIR:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23070·2022-12-15

    Samnyte Tattoo Numbing Cream Recalled for Non-Child-Resistant Packaging

    Samnyte Tattoo Numbing Cream is recalled because its packaging does not meet child-resistant requirements under federal law. The product contains lidocaine and poses a poisoning risk if ingested by young children.

    Product
    Samnyte Tattoo Numbing Creams
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23072·2022-12-15

    Good Matters Three-Wick Candles Recalled for Fire and Laceration Hazards

    About 30,100 Good Matters three-wick candles are being recalled because the candles can burn at higher than usual temperatures, causing glass jars to break and posing fire and laceration injury risks.

    Product
    Good Matters Three-Wick Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23069·2022-12-15

    Rosso Motors Youth ATVs Recalled for Federal Safety Standard Violations

    Rosso Motors is recalling approximately 2,800 eQuad X and eQuad Q youth ATVs sold online from June 2019 through April 2021 because they violate federal safety standards and pose a risk of serious injury or death.

    Product
    Rosso Motors eQuad X and eQuad Q Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V931000·2022-12-15

    Windshield wiper failure recall affects 2023 Jayco Seneca and Entegra motorhomes

    Jayco and Entegra are recalling 2023 motorhomes because windshield wiper arms may break, causing wiper failure. This reduces visibility and increases crash risk in wet driving conditions.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23718·2022-12-15

    ESS Universal Waterproof Foam Mattresses Recalled for Flammability Violation

    ESS Universal USA is recalling approximately 1,800 Waterproof Foam Mattresses sold online from April 2021 through March 2022 because they fail to meet mandatory federal flammability standards, posing a fire hazard.

    Product
    Waterproof Foam Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V929000·2022-12-15

    2023 GMC Terrain and Chevrolet Equinox Passenger Airbag Detection Recall

    GM is recalling certain 2023 GMC Terrain and Chevrolet Equinox vehicles with ventilated front passenger seats. The occupant detection system may fail to disable the airbag when a child is present, increasing crash injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23068·2022-12-15

    Jacuzzi and Sundance Hot Tubs Recalled for Thermal Burn Hazards

    Sundance Spas is recalling certain Jacuzzi and Sundance brand hot tubs because the temperature sensor may relay incorrect water temperatures, causing water hotter than the set temperature and posing burn and heat stroke hazards. No injuries have been reported.

    Product
    Jacuzzi® Hot Tubs and Sundance® Spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V932000·2022-12-15

    Travel trailer window glass separation risk in Airstream Basecamp models

    Airstream is recalling certain 2017-2022 Basecamp travel trailers because the adhesive bond between the glass and frame of the entry door window can fail, causing glass separation and potentially increasing injury or crash risk.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23073·2022-12-15

    SIMU DMI6 Hz Motors for Awnings and Shutters Recalled for Electric Shock Hazard

    SIMU is recalling approximately 13,800 DMI6 Hz motors used in motorized awnings and shutters because the power cable can disconnect during manual operation, creating an electric shock and electrocution hazard.

    Product
    SIMU DMI6 Hz motors sold with awnings and shutters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23071·2022-12-15

    Gabby D-Ring Fritz Mirrors Recalled Due to Fall and Laceration Hazards

    Gabriella White LLC (Gabby Home) is recalling approximately 930 D-Ring Fritz wall mirrors because the hanging mechanism can fail, causing the mirror to detach and fall from the wall. No injuries have been reported, but seven detachment incidents have occurred.

    Product
    D-Ring Fritz Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23717·2022-12-15

    Crate and Barrel Thornhill Baby Cribs Recalled for Fall Hazard

    Crate and Barrel is recalling about 280 Thornhill baby cribs because mattress support pins can become loose or not fit properly, causing the mattress to fall. The firm received six reports of the mattress support pins not fitting correctly or falling out, though no injuries have been reported.

    Product
    Thornhill Dark Brown and Natural Baby Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0330-2023·2022-12-14

    Sensititre Medical Device Recall: False Antibiotic Susceptibility Test Results

    Remel Inc. is recalling Sensititre HPB1 diagnostic plates that may produce false susceptible results for specific bacteria when tested with seven antibiotics. This could lead to inaccurate susceptibility information affecting clinical treatment decisions.

    Product
    Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2023·2022-12-14

    Medical Device Recall: Sensititre Test Produces False Antibiotic Susceptibility Results

    Remel Inc. is recalling a diagnostic test that may incorrectly report antibiotic susceptibility in certain Gram-negative bacteria. False results could lead to inappropriate antibiotic treatment.

    Product
    Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V927000·2022-12-14

    Audi Recalls 2022 E-Tron GT Models Due to Suspension Strut Defect

    Audi is recalling 96 2022 E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.

    Product
    AUDI — AUDI E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V926000·2022-12-14

    Polestar Recalls 2020-2021 Polestar 1 Vehicles for Battery Fire Risk

    Polestar is recalling 2020-2021 Polestar 1 vehicles because defective high-voltage battery cells may overheat and cause a fire. Dealers will replace the cells.

    Product
    POLESTAR — POLESTAR POLESTAR 1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0339-2023·2022-12-14

    CAIRE Liberator 20 Liquid Oxygen System Recalled for Weld Defects

    Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.

    Product
    CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0327-2023·2022-12-14

    Thermo Sensititre diagnostic plate recalled for false susceptibility results

    Sensititre diagnostic plates may give false antibiotic susceptibility results for certain bacteria species, potentially affecting treatment decisions. The FDA issued a Class I recall for approximately 1,917 units distributed nationwide.

    Product
    Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0332-2023·2022-12-14

    FDA Class I Recall: Thermo Sensititre Gram Negative Diagnostic Test Inaccuracy

    Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.

    Product
    Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0338-2023·2022-12-14

    FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units

    Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.

    Product
    CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide