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.

49301–49325 of 80977

  • SevereFDA (Drugs)·D-0462-2017·2017-02-08

    VistaPharm Recalls Lactulose Solution Due to Potential Bacterial Contamination

    VistaPharm is recalling Lactulose Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Lactulose Solution, USP 20 g/30 mL, 50 unit dose cups of 30 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-038-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2017·2017-02-08

    VistaPharm Recalls Lactulose Solution Due to Potential Bacterial Contamination

    VistaPharm is recalling Lactulose Solution USP because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Lactulose Solution, USP 10 g/15 mL, 50 unit dose cups of 15 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-039-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1409-2017·2017-02-08

    Houdini Inc. Recalls Vintners Path Cabernet Baskets Due to Salmonella Risk

    Houdini Inc. is recalling Vintners Path Cabernet Seasons Greetings Baskets due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    Vintners Path Cabernet Seasons Greetings Basket #763
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V079000·2017-02-08

    Mercedes-Benz Recalls 2016 GLE350 and GLS450 for Windshield Bonding Defect

    Mercedes-Benz is recalling 2016 GLE350 and GLS450 vehicles because insufficient windshield bonding may cause the glass to separate in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE350, GLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0466-2017·2017-02-08

    VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination

    VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1401-2017·2017-02-08

    Houdini Inc. Recalls Wine and Champagne Baskets Due to Salmonella Risk

    Houdini Inc. is recalling 16 baskets of The Ultimate Wine and Champagne Collection #399 due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    The Ultimate Wine and Champagne Collection Basket #399
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1414-2017·2017-02-08

    Houdini Inc. Recalls Napa and Sonoma Duet Basket #973 for Salmonella Risk

    Houdini Inc. is recalling 19 Napa and Sonoma Duet Basket #973 units due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    Napa and Sonoma Duet Basket #973
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0460-2017·2017-02-08

    VistaPharm Recalls Phenytoin Oral Suspension Due to Water Contamination

    VistaPharm is recalling Phenytoin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Phenytoin Oral Suspension, USP 100 mg/ 4 mL, 50 unit dose cups of 4 mL per case., Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-036-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0461-2017·2017-02-08

    VistaPharm Recalls Nystatin Oral Suspension Due to Water Contamination

    VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL per case (NDC No. 66689-037-50), b). 100 unit dose cups of 5 mL per case (NDC 66689-037-99), Rx only, Manufactured by VistaPharm, Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0457-2017·2017-02-08

    VistaPharm Recalls Nystatin Oral Suspension Due to Potential Water Contamination

    VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 bottles per case (NDC 66689-008-02), b) 16 fl. oz. (237 mL), 12 bottles per case (NDC 66689-008-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V077000·2017-02-08

    Mercedes-Benz Recalls 2017 GLE and GLS Models for Center Console Defect

    Mercedes-Benz is recalling 2017 GLE and GLS models because the center console may unlatch in a crash, allowing objects to strike occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS550, GLE550E, AMG GLS63, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1397-2017·2017-02-08

    Houdini Inc. Recalls Napa & Sonoma Valley Exclusive Basket #141 for Salmonella

    Houdini Inc. is recalling 79 Napa & Sonoma Valley Exclusive Basket #141 units due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    Napa & Sonoma Valley Exclusive Basket #141
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0467-2017·2017-02-08

    VistaPharm Recalls Methadone Hydrochloride Oral Concentrate Due to Water Contamination

    VistaPharm is recalling 3,354 bottles of Methadone Hydrochloride Oral Concentrate because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-711-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0449-2017·2017-02-08

    Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures

    Dr. Reddy's Laboratories is recalling Flucanazole tablets because they failed dissolution and stability specifications.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1133-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 275 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 900-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0459-2017·2017-02-08

    VistaPharm Recalls Metoclopramide Oral Solution Due to Potential Water Contamination

    VistaPharm is recalling specific lots of Metoclopramide Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1108-2017·2017-02-08

    PerkinElmer Spare Disk Remover Module Recall Due to Corrosion Risk

    PerkinElmer is recalling Spare Disk Remover Modules because defective axles may corrode in humid conditions, potentially contaminating test plates.

    Product
    Spare Disk Remover Module; Product Number: 61001820 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·17V080000·2017-02-08

    Mercedes-Benz Recalls 2017 Models for Air Bag Ignition Failure

    Mercedes-Benz is recalling 2017 E300, E400, E550, GLA 250, and CLA250 vehicles because the pelvis or front passenger air bag inflator may fail to ignite in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, E400, GLA 250, CLA250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1107-2017·2017-02-08

    PerkinElmer Genetic Screening Processor Recalled for Corroding Axles

    PerkinElmer is recalling 24 Genetic Screening Processor instruments because defective ball bushing axles may corrode in humid conditions, risking contamination of sample wells.

    Product
    Genetic Screening Processor (GSP); PerkinElmer Part Number= 2021-0010 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1122-2017·2017-02-08

    Mevion S250 Proton Therapy Units Recalled for Data Loss Error

    Mevion Medical Systems is recalling two S250 Proton Radiation Therapy units because a software error can cause Delta corrections to be lost.

    Product
    MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1364-2017·2017-02-08

    Rich Products Recalls Ice Cream Layer Cakes Due to Undeclared Walnuts

    Rich Products Corp. is recalling specific Jon Donaire Ice Cream Layer Cakes because they may contain undeclared walnuts from a supplier.

    Product
    Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy vanilla ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 62878 6 (retail), Product Code 62878, and UPC 0 49800 02453 3 (retail), Product Code 02453 --- Rich Products Corp., Buffalo, NY 14213…
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1128-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall affects 180 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 777-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide