The Recall Desk

State

South Carolina product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55551–55575 of 80986

  • SevereCPSC·16096·2016-02-04

    CE North America Recalls KUL Fan Heaters Due to Fire Hazard

    CE North America is recalling KUL portable fan heaters sold at Bed Bath & Beyond because they can overheat and catch fire. Four fire incidents have been reported, with no injuries.

    Product
    KUL Fan Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E009000·2016-02-04

    Takata Recalls Side Air Bag Inflators Due to Rupture Risk

    Takata is recalling specific side air bag inflators manufactured in December 2014 because a manufacturing error could cause them to rupture and propel metal fragments into the vehicle.

    Product
    AIR BAGS:SIDE/WINDOW recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16095·2016-02-04

    Wedgwood Decorative Baby Rattles Recalled Due to Choking Hazard

    WWRD is recalling Wedgwood Peter Rabbit decorative baby rattles because ball bearings can release, posing a choking hazard to young children.

    Product
    Wedgwood Peter Rabbit decorative baby rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E010000·2016-02-04

    Helmet City Recalls Model 115 Helmets Due to Strap Stretching

    Helmet City, Inc. is recalling 270 Model 115 German helmets, size XL, because the straps may stretch excessively during a crash, failing to keep the helmet secured.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V061000·2016-02-03

    Honda and Acura Recall Vehicles Due to Airbag Inflator Rupture Risk

    Honda is recalling specific 2005-2016 Acura and Honda vehicles because the driver's airbag inflator may rupture during a crash, potentially causing serious injury or death.

    Product
    ACURA — ACURA, HONDA RL, RIDGELINE, RDX, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0689-2016·2016-02-03

    Cook Medical Recalls Zilver 518RX Vascular Stent Delivery Systems

    Cook Medical is recalling 753 Zilver 518RX Vascular Stent delivery systems because a manufacturing defect may cause the catheter joint to separate during use.

    Product
    Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0592-2016·2016-02-03

    Pharmakon Recalls Succinylcholine Syringes Due to Stability Data Concerns

    Pharmakon Pharmaceuticals is recalling 2,750 syringes of Succinylcholine 20 mg/mL because stability data does not support the expiration dates.

    Product
    Succinylcholine 20 mg/mL, injectable packed in syringes, Total dosage 100 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·16090·2016-02-03

    Rockwood Multi-Function Power Packs Recalled Due to Fire Hazard

    Eastwood is recalling Rockwood power packs because their lithium-ion batteries can burst during charging, posing a fire hazard.

    Product
    Rockwood Multi-function power packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V063000·2016-02-03

    GM Recalls Saab and Saturn Vehicles for Air Bag Inflator Defect

    General Motors is recalling specific Saab and Saturn vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    SAAB — SAAB, SATURN 9-5, ASTRA, 9-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V060000·2016-02-03

    Subaru Recalls Tribeca Vehicles for Hood Safety System Malfunction

    Subaru is recalling 2006-2014 Tribeca vehicles because the hood may open unexpectedly while driving, potentially blocking the driver's view.

    Product
    SUBARU — SUBARU TRIBECA, B9 TRIBECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0598-2016·2016-02-03

    Pharmakon Recalls Hydromorphone Syringes Due to Stability Data Issues

    Pharmakon Pharmaceuticals is recalling 8,000 units of Hydromorphone HCl 1 mg/mL syringes nationwide because stability data does not support the expiration dates.

    Product
    Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 1 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0589-2016·2016-02-03

    Pharmakon Recalls Subpotent Epinephrine Injectable Syringes Nationwide

    Pharmakon Pharmaceuticals is recalling 1,150 syringes of Epinephrine (PF) 10 mcg/mL because the drug was found to be subpotent. The recall is voluntary and nationwide.

    Product
    Epinephrine (PF) 10 mcg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 50 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0593-2016·2016-02-03

    Pharmakon Recalls Subpotent Midazolam Injectable Syringes Nationwide

    Pharmakon Pharmaceuticals is recalling 210 syringes of Midazolam (PF) 0.5 mg/mL because the drug is subpotent. The recall is voluntary and nationwide.

    Product
    Midazolam (PF) 0.5 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 0.5 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0651-2016·2016-02-03

    Midmark Vantage Panoramic X-Ray System Recalled for Collimator Failure

    Midmark Corp dba Progeny Inc is recalling 832 Vantage Panoramic X-Ray Systems because a primary collimator failure may cause unintentional movement without an error message.

    Product
    Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray System is a class II extra oral X-Ray system used to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw and oral structures.…
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-0693-2016·2016-02-03

    Fresenius Liberty Cycler Peritoneal Dialysis Machines Recalled for Door Latch Defect

    Fresenius Medical Care is recalling 14,094 Liberty Cycler peritoneal dialysis machines because the door latch may not fully close, posing a risk of injury or treatment delay.

    Product
    Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and RTLR180111
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V062000·2016-02-03

    Forest River Recalls 2016 Surveyor RVs Due to Wiring Defect

    Forest River is recalling 12 model year 2016 Surveyor recreational vehicles because incorrect wiring may allow excessive current, posing an electrocution risk.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0695-2016·2016-02-03

    Bio-Rad D-10 Rack Loader Recalled for Potential Sample ID Error

    Bio-Rad is recalling D-10 Rack Loaders because a rare configuration issue could assign patient results to incorrect sample IDs.

    Product
    D-10 Rack Loader; Model Number 220-0600; Hematology: The D-10 is a fully integrated system for sample dilution, processing and analysis of hemoglobin, designed for use with specific Bio-Rad reagent kits. The D-10 incorporates the use of a dedicated software system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16091·2016-02-03

    Lutron Recalls Roller Shades Due to Falling Impact Hazard

    Lutron Electronics is recalling about 30,000 Serena and SIVOIA QS TRIATHLON roller shades because they can fall from brackets, posing an impact hazard.

    Product
    Roller Shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide