The Recall Desk

State

South Carolina product recalls

73,741 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,152
Critical
1,275
Severe
2,169
Most recent
2026-10-28

Of the 7,152 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,169 (30%) are Severe.

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39401–39425 of 80893

  • ModerateFDA (Drugs)·D-0296-2019·2018-12-19

    LGM Pharma Recalls Thyroid Powder Due to Inconsistent Active Ingredient Levels

    LGM Pharma LLC is recalling 1,307 kg of Thyroid Powder, USP, because the product has inconsistent levels of active ingredients levothyroxine and liothyronine.

    Product
    Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0597-2019·2018-12-19

    COVIDIEN Recalls Salem Sump Stomach Tubes Due to Packaging Error

    COVIDIEN LLC is voluntarily recalling 1,522 Salem Sump Dual Lumen Stomach Tubes because one lot of 10 Fr tubes was incorrectly packaged in 16 Fr pouches.

    Product
    Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm), Product Code 8888264911 Product Usage: The Salem Sump Tubes are intended for decompression and drainage of stomach contents following injury, illness, or surgery in patients with intestinal obstruction, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0601-2019·2018-12-19

    Tosoh Recalls Hemoglobin A1c Control Material Due to Potential Degradation

    Tosoh Bioscience is recalling Hemoglobin A1c Control material due to potential degradation that may cause testing delays.

    Product
    Hemoglobin A1c Control, Part no. 220232 for use as quality control material to monitor the precision of laboratory testing procedures for HbA1c quantitation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V894000·2018-12-18

    Ford Recalls F-Series Trucks Due to Block Heater Fire Risk

    Ford is recalling 410,289 F-Series trucks because water in the block heater cable can cause corrosion and a fire.

    Product
    FORD — FORD F-150, F-450, redundant F-350, redundant F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V926000·2018-12-18

    Eldorado Buses Recalled for Back Seat Cushion Locking Defect

    Eldorado is recalling 2017-2018 Arrivo, Passport, and E-Z Rider Max BRT buses because back seat cushions may not stay locked in place during a crash.

    Product
    ELDORADO — ELDORADO ARRIVO, PASSPORT, E-Z RIDER MAX BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19052·2018-12-18

    TerraTrike Rambler E.V.O. Adult Tricycles Recalled for Crash Hazards

    TerraTrike is recalling about 450 Rambler E.V.O. adult tricycles because the torque sensor can activate unexpectedly, causing the trike to power forward and posing crash and injury hazards.

    Product
    TerraTrike Rambler E.V.O adult tricycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V925000·2018-12-18

    Triple E Recalls 2019 Serenity RVs Due to Battery Fire Risk

    Triple E is recalling 2019 Serenity recreational vehicles because a metal cable may contact the battery terminal, creating a fire hazard.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V893000·2018-12-17

    Audi Recalls 2018 A5 Sportback for Loose Front Suspension Fasteners

    Volkswagen is recalling 2018 Audi A5 Sportback vehicles because front suspension fasteners may not be sufficiently tightened, which could cause a front wheel to become loose.

    Product
    AUDI — AUDI A5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V896000·2018-12-17

    Heartland Milestone Recalled for Improperly Secured Propane Hose

    Heartland is recalling 2019 Milestone trailers because a propane hose may be improperly secured, posing a fire risk if it contacts the tire.

    Product
    HEARTLAND — HEARTLAND MILESTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V892000·2018-12-17

    Blue Bird Recalls 2017-2019 Vision School Buses for Air Compressor Belt Defect

    Blue Bird is recalling 2017-2019 Vision school buses with specific Cummins engines because a slipping air compressor belt may cause the parking brake to apply while driving, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·122-2018·2018-12-15

    Mannarich Recalls Siluriformes Fish Products Lacking Import Inspection

    Mannarich Food, Inc. is recalling approximately 145,245 pounds of Siluriformes fish products that were imported from Malaysia without U.S. inspection.

    Product
    Mannarich Food, Inc. Recalls Siluriformes Products Produced without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V889000·2018-12-14

    Autocar Recalls 2019 Xpeditor Vehicles Due to Loose Driveline Bolts

    Autocar is recalling 2019 Xpeditor vehicles because universal joint strap bolts may not be properly tightened, which could cause the drive shaft to detach and increase crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V891000·2018-12-14

    Hyundai Recalls 2018 Elantra GT for Sunroof Obstacle Detection Defect

    Hyundai is recalling 2018 Elantra GT vehicles because the panoramic sunroof motor may be incorrectly programmed, preventing it from detecting obstacles while closing.

    Product
    HYUNDAI — HYUNDAI ELANTRA GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V888000·2018-12-13

    Toyota Recalls 2018-2019 Tacoma Vehicles Due to Brake Master Cylinder Defect

    Toyota is recalling 2018-2019 Tacoma vehicles because improper machining of the brake master cylinder may damage internal seals, potentially reducing brake performance and increasing crash risk.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V887000·2018-12-13

    Toyota Recalls Land Cruiser and Lexus LX 570 for Air Bag Deactivation Risk

    Toyota is recalling 2008-2019 Land Cruiser and Lexus LX 570 vehicles because a broken wire harness may deactivate front passenger air bags, increasing injury risk in crashes.

    Product
    TOYOTA — TOYOTA, LEXUS LAND CRUISER, LX570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E115000·2018-12-13

    Lifeworks Recalls Heated Seat Cushions and Blankets Due to Fire Risk

    Lifeworks is recalling specific Armor All heated seat cushions and blankets sold at Meijer because they may overheat and melt, posing a fire and injury risk.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19050·2018-12-13

    TJX Recalls Glass and Ceramic Drawer Knobs Due to Laceration Hazard

    TJX is recalling glass and ceramic drawer knobs sold at T.J. Maxx, Marshalls, and HomeGoods because they can shatter when pulled, posing a laceration hazard.

    Product
    Glass and ceramic drawer knobs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V890000·2018-12-13

    Frazer Recalls 2017-2018 Ambulances Due to Brake Light Wiring Issue

    Frazer is recalling 2017-2018 Type 1 and Type 3 ambulances and Mobile Stroke Units because Whelen accessory brake lights may illuminate without the brake pedal being pressed.

    Product
    FRAZER — FRAZER TYPE 1 AMBULANCE, TYPE 3 AMBULANCE, MOBILE STROKE UNIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2019·2018-12-12

    Fresenius Kabi Recalls Sodium Chloride Vials Due to Incorrect Latex Labeling

    Fresenius Kabi is recalling 1,312,350 vials of Sodium Chloride Injection because labels incorrectly state the stoppers do not contain natural rubber latex.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide