The Recall Desk

State

South Carolina product recalls

73,827 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,153
Critical
1,275
Severe
2,170
Most recent
2026-11-04

Of the 7,153 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 2,170 (30%) are Severe.

These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53201–53225 of 80980

  • ModerateNHTSA·16V516000·2016-07-07

    GM Recalls 2016-2017 Buick Envision for Incorrect Tire Label Weight

    General Motors is recalling 2016-2017 Buick Envision vehicles because the Tire and Loading Information label may display incorrect maximum weight information, which could lead to vehicle overloading.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1592-2016·2016-07-06

    Kroger Simple Truth Organic Mixed Vegetables Recalled for Listeria Risk

    The Kroger Co is recalling Simple Truth Organic Mixed Vegetables because the supplier reported possible Listeria monocytogenes contamination.

    Product
    simple truth organic Mixed Vegetables NET WT 10 OZ (283g) KEEP FROZEN INGREDIENTS: ORGANIC CARROTS, ORGANIC CORN ORGANIC PEAS, GREEN BEANS.
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-1595-2016·2016-07-06

    Maytag Blue Cheese Recalled Due to Listeria monocytogenes Contamination

    Maytag Dairy Farms is recalling Maytag Blue Cheese products because they are contaminated with Listeria monocytogenes. The recall covers various wheel, wedge, and crumble sizes distributed nationwide.

    Product
    Maytag Blue Cheese. Wedges and wheels are packaged in an aluminum foil wrapper and shipped in cardboard box. The wedges and wheels are packaged in the following sizes: 1) 4 LB. wheel, UPC 8 54089 00114 0; 2) 2 LB. wheel, UPC 8 54089 00112 6; 3) 1 oz. wedges, UPC 8 54089…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1597-2016·2016-07-06

    Mccall Farms Recalls Piggly Wiggly Yellow Cut Corn for Listeria Risk

    Mccall Farms is recalling Piggly Wiggly Yellow Cut Corn due to possible Listeria monocytogenes contamination. The product was distributed in South Carolina.

    Product
    Piggly Wiggly, Yellow Cut Corn, Net Wt 32oz (2 lbs), 907g bags, Distributed by Piggly Wiggly LLC, Keene, NH 03431.
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·16215·2016-07-06

    Razor Recalls Hoverboards Due to Fire and Explosion Risk

    Razor USA is recalling about 28,000 Hovertrax hoverboards because their lithium-ion batteries can overheat, smoke, catch fire, or explode.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1588-2016·2016-07-06

    Ross Chocolates Recalls Dark Chocolate Bars for Undeclared Milk Allergen

    Ross Chocolates is recalling 4,128 bars of No Sugar Added Dark Chocolate because the labels failed to declare the possible milk allergen.

    Product
    R No Sugar Added; Dark Chocolate 34 g/1.2 oz. Ross Chocolates, 4061 Butters Road, Scotch Creek, BC UPC 726007100054 Best Before: 191018
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·16210·2016-07-06

    Hoverboard LLC Recalls Self-Balancing Scooters Due to Fire Hazard

    Hoverboard LLC is recalling Powerboard self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode. No injuries have been reported, but one instance of property damage occurred.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2100-2016·2016-07-06

    Physio-Control Recalls LIFEPAK AEDs Due to Shock Delivery Failure Risk

    Physio-Control is recalling LIFEPAK CR Plus and EXPRESS AEDs because a faulty component may prevent the device from delivering a shock during cardiac arrest.

    Product
    LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External Defibrillator(s) and are non-wearable. LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators are intended for use on patients in cardiac arrest.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·16214·2016-07-06

    Overstock Recalls Self-Balancing Scooters Due to Fire Hazard

    Overstock.com is recalling about 4,300 self-balancing scooters sold online from September to December 2015 because their lithium-ion batteries can overheat and catch fire.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16211·2016-07-06

    Swagway Recalls Self-Balancing Scooters Due to Fire and Explosion Hazards

    Swagway is recalling X1 hoverboards because their lithium-ion batteries can overheat, smoke, catch fire, or explode. Consumers should stop using the units and contact Swagway for a repair or credit.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16218·2016-07-06

    Ten Firms Recall Self-Balancing Scooters Due to Fire and Explosion Hazards

    Ten companies are recalling about 501,000 self-balancing scooters because their lithium-ion batteries can overheat, catch fire, or explode. Consumers should stop using these products immediately.

    Product
    Self-Balancing Scooters/Hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2060-2016·2016-07-06

    Hospira Recalls PlumSet IV Administration Sets Due to Fluid Leakage

    Hospira is recalling PlumSet IV administration sets because intravenous fluid may leak at the secondary port. The recall covers 3,920,932 units distributed in the US and Canada.

    Product
    *** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, Non-Vented, 110 Inch, Non-DEHP; Product Usage: The CLAVE of the secondary port is used as an easy secondary access that allows concurrent and piggyback mode…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V512000·2016-07-06

    Newmar Recalls 2017 Motorhomes Due to Front Fascia Wood Trim Separation Risk

    Newmar is recalling 152 model year 2017 motorhomes because front fascia wood trim may separate and contact occupants, potentially causing loss of vehicle control.

    Product
    NEWMAR — NEWMAR DUTCH STAR, KING AIRE, MOUNTAIN AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16216·2016-07-06

    Keenford Recalls iMoto Hoverboards Due to Fire and Explosion Risks

    Keenford Limited is recalling about 84,000 iMoto self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2064-2016·2016-07-06

    CareFusion Alaris System PC Unit Recall for Incorrect Patient Weight Data

    CareFusion 303, Inc. is recalling 69,693 Alaris System PC Units because the RESTORE feature may incorrectly populate patient weight for specific infusion modules.

    Product
    Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2053-2016·2016-07-06

    Nephron Recalls Sodium Chloride Inhalation Solution Due to Sterility Concerns

    Nephron Pharmaceuticals is recalling 11,208 cartons of Sodium Chloride Inhalation Solution because internal dye tests failed to confirm vial integrity.

    Product
    Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is…
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-2056-2016·2016-07-06

    Hospira Symbiq Infusion Pumps Recalled for False Occlusion Alarms

    Hospira is recalling Symbiq Two Channel Infusers due to frequent false occlusion alarms that may delay or interrupt patient therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16217·2016-07-06

    Hype Wireless Recalls Self-Balancing Scooters Due to Fire Hazard

    Hype Wireless is recalling about 25,000 Roam brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of smoking, fire, or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2092-2016·2016-07-06

    Smith & Nephew Legion Hinge Knee Femoral Assembly Recall

    Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 4 LEFT, A/P 58.5 MM, M/L 66 MM, REF 71421374 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2016·2016-07-06

    Medical Depot Recalls Aluminum Crutches Due to Tip Failure

    Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail and detach from the ground.

    Product
    Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16208·2016-07-06

    PTX Performance Products Recalls Airwalk Hoverboards Due to Fire Hazard

    PTX Performance Products is recalling about 4,900 Airwalk self-balancing scooters because the lithium-ion batteries can overheat, posing a risk of fire or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2085-2016·2016-07-06

    Medtronic Recalls Sagittal Saw Devices Due to Potential Fluid Leakage

    Medtronic is recalling 368 Sagittal Saw devices because testing identified a potential for fluid leakage into the motor during use.

    Product
    Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital, Finger Catalog Number: ES310; Saw Saggital, Finger Refurbished Catalog Number: ES310-R; Used to dissect bone in surgical applications.
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Devices)·Z-2062-2016·2016-07-06

    Hospira Recalls LifeShield IV Sets Due to Potential Fluid Leakage

    Hospira is recalling approximately 3.9 million LifeShield IV administration sets because fluid may leak at the secondary port.

    Product
    *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, CONVERTIBLE PIN, CLAVE SECONDARY PORT, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 118 IN; PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: List No. 19685-28…
    Category
    Medical Device
    Distribution
    Distributed nationwide