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.

50376–50400 of 80977

  • SevereFDA (Devices)·Z-0653-2017·2016-11-30

    AtriCure Recalls COBRA Fusion Ablation Systems Due to Component Separation Risk

    AtriCure is recalling COBRA Fusion Ablation Systems because a part may separate and remain in the body, potentially causing permanent impairment or damage.

    Product
    COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model Numbers: 700-001, 700-001S, 700-001MI, 700-002, and 700-003. Intended to ablate cardiac tissue during cardiac surgery using radiofrequency (RF) energy when…
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-0527-2017·2016-11-30

    Free2b Sun Cups Chocolate Recalled for Potential Milk Contamination

    Seth Ellis Chocolatier is recalling Free2b Sun Cups Chocolate due to potential contamination with milk ingredients. The recall covers 189 master cases distributed nationwide.

    Product
    Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged in 2 Cups. Net weight 1.5 oz (45g) and 1 Cup. Net weight 0.75 oz (21g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0146-2017·2016-11-30

    VistaPharm Recalls Lactulose Solution Due to Bacterial Contamination

    VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.

    Product
    Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0512-2017·2016-11-30

    CSM Bakery Recalls 7-Eleven Sugar Cookie Base for Undeclared Peanut

    CSM Bakery Products NA is recalling 7-Eleven Sugar Cookie Base, 50#, because it contains undeclared peanut protein. The product was distributed across 19 states and two territories.

    Product
    7-Eleven Sugar Cookie Base, 50#
    Category
    Food
    Distribution
    19 states
  • HighFDA (Devices)·Z-0635-2017·2016-11-30

    Merit Medical Procedure Kits Recalled for Compromised Sterile Barrier

    Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.

    Product
    Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0655-2017·2016-11-30

    Hologic Recalls SURESOUND22 Uterine Sounds Due to Sterile Barrier Breach

    Hologic is recalling SURESOUND22 uterine sound multipacks because a breach in the sterile barrier compromises product sterility.

    Product
    SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices. For uterine sound
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0530-2017·2016-11-30

    EN-R-G Foods Recalls Protein Chews Due to Nausea and Vomiting Complaints

    EN-R-G Foods is recalling Cherry Lime, Raspberry, and Juneberry Protein Chews due to consumer complaints of nausea and vomiting after consumption.

    Product
    Protein Chews Raspberry,1.8oz, film package, 12 packets per box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0632-2017·2016-11-30

    Merit Medical Recalls Manifold Kits Due to Compromised Sterile Barrier

    Merit Medical Systems is recalling 40 Manifold Kits (Catalog No. K09-11867AP) because the sterile barrier is compromised, posing a risk of infection.

    Product
    Manifold Kit. Catalog Number K09-11867AP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0520-2017·2016-11-30

    CSM Bakery Cream Cake Mix Recalled for Undeclared Peanut Allergen

    CSM Bakery Products NA is recalling 38260 Cream Cake Mix because it contains undeclared peanut protein. The product was distributed in 19 states and two territories.

    Product
    38260 Cream Cake Mix, 50#
    Category
    Food
    Distribution
    19 states
  • HighFDA (Devices)·Z-0634-2017·2016-11-30

    Merit Medical Recalls Pressure Monitoring Kits Due to Sterile Barrier Compromise

    Merit Medical Systems is voluntarily recalling 130 MeriTrans Pressure Monitoring Kits because a compromised sterile barrier may affect product sterility.

    Product
    Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0622-2017·2016-11-30

    Toshiba Aquilion Prime CT System Recalled for Cooling Oil Leak Risk

    Toshiba American Medical Systems is recalling Aquilion Prime CT systems because cooling oil in the x-ray tube heat exchanger may leak during operation.

    Product
    Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT system with an 40-row detector. High-speed rotation allows rapid data acquisition and shortens scan times, while the fast reconstruction unit further improves throughput, reducing the time required for diagnosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V861000·2016-11-30

    Cummins Recalls 2015-2016 Generator Sets Due to Door Hinge Failure Risk

    Cummins is recalling 164 model year 2015-2016 generator sets because door hinges may fail, causing doors to detach and create road hazards.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0375-2017·2016-11-30

    Philips CT Scanner Recall Due to Tabletop Movement Failure

    Philips is recalling 1,363 CT scanners because the patient support tabletop may fail to move horizontally during scans due to a mechanical linkage failure.

    Product
    Philips Healthcare System X-ray Tomography Computed :
    Category
    Medical Device
    Distribution
    Distributed nationwide