The Recall Desk

State

South Carolina product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49876–49900 of 80977

  • HighCPSC·17064·2017-01-04

    Toshiba Laptop Battery Packs Recalled for Overheating and Fire Hazards

    Toshiba is expanding a recall of Panasonic lithium-ion battery packs for laptops due to overheating, burn, and fire risks. No injuries have been reported.

    Product
    Panasonic battery packs used in Toshiba laptop computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1082-2017·2017-01-04

    Publix Banana-Flavored Pancake Mix Recalled for Salmonella Risk

    Publix is recalling its Premium Banana-Flavored Chocolate Chip Pancake & Waffle Mix because the milk powder ingredient may contain Salmonella.

    Product
    Publix Premium Banana-Flavored Chocolate Chip Pancake & Waffle Mix, 16 oz box.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0921-2017·2017-01-04

    Siemens Recalls CT Systems for Potential Power Cutout Defect

    Siemens is recalling 13 SOMATOM Perspective CT systems to replace a component that could cause power cutouts during use.

    Product
    SOMATOM Perspective, Computed tomography x-ray system
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0909-2017·2017-01-04

    GE Healthcare Recalls Legacy Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    Legacy
    Category
    Medical Device
    Distribution
    41 states
  • ModerateFDA (Devices)·Z-0902-2017·2017-01-04

    PerkinElmer Recalls Specimen Gate Laboratory Software Due to Disk Space Issue

    PerkinElmer Health Sciences is recalling 21 units of Specimen Gate Laboratory and eReports software because a defect may cause excessive disk space consumption, leading to software failure.

    Product
    Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is intended for use as a data processing software used in the storage, retrieving, and processing of laboratory data. Specimen Gate eReports Software is a module…
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Food)·F-0906-2017·2017-01-04

    Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage

    Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.

    Product
    Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Virt-Select Prenatal Softgels Due to GMP Deviations

    Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.

    Product
    Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0903-2017·2017-01-04

    Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.

    Product
    VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0917-2017·2017-01-04

    Shimadzu X-ray TV System Recalled for Oil Leak Risk

    Shimadzu Medical Systems is recalling 39 SONIALVISION G4 X-ray TV Systems due to a potential oil leak from the x-ray tube housing.

    Product
    Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Drugs)·D-0241-2017·2017-01-04

    VirtPrex Prenatal Tablets Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0235-2017·2017-01-04

    Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects

    Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.

    Product
    Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0239-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Extra-Virt Plus DHA Prenatal Softgels

    Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.

    Product
    Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0238-2017·2017-01-04

    Virt-Advance Prenatal Softgels Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E001000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Rupture Recall

    Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E002000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Module Recall

    Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V002000·2017-01-03

    Audi Recalls 2012-2017 Models for Coolant Pump Fire Risk

    Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.

    Product
    AUDI — AUDI A6, A4 ALLROAD, Q5, A5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V001000·2017-01-03

    Audi Recalls 2011-2017 Q5 Vehicles Due to Side Air Bag Corrosion Risk

    Volkswagen Group of America is recalling 2011-2017 Audi Q5 vehicles because water in the sunroof drainage system may corrode side air bag inflators, posing a risk of serious injury.

    Product
    AUDI — AUDI Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V957000·2016-12-31

    Forest River Recalls 2017 Fifth-Wheel RVs Due to Door Hinge Defect

    Forest River is recalling 2017 XLR Toyhauler and Prime Time Spartan fifth-wheel vehicles because rear cargo door hinge welds may be insufficient, increasing the risk of personal injury.

    Product
    PRIME TIME — PRIME TIME, FOREST RIVER SPARTAN, XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide