The Recall Desk

State

South Carolina product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49076–49100 of 80970

  • CriticalFDA (Food)·F-1503-2017·2017-03-01

    Palmer's Candies Christmas Tree Pretzels Recalled for Salmonella Risk

    Palmer's Candies is recalling Christmas Tree Pretzels because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Bakery Delights Christmas Tree Pretzels NET WT 5 OZ (141 g) packaged in foil bags, UPC Code 77232-13227
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1511-2017·2017-03-01

    Palmer's Candies Heart Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 54 cases of Palmer's Candies Chocolatey Flavored NP Heart Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Flavored NP Heart Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10778
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1495-2017·2017-03-01

    Palmer's Candies Chocolate Almond Bark Recalled for Salmonella Risk

    Palmer and Company is recalling specific chocolate almond bark products because an ingredient may be contaminated with Salmonella.

    Product
    A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC 77232-17250; B) Publix Bakery Almond Bark with Cocoa, NET WT 10 OZ (283 g), packaged in paper bags, UPC 77232-22691; C) Palmer's Candies Chocolate Almond Bark, 10 lbs.…
    Category
    Food
    Distribution
    34 states
  • SevereNHTSA·17V130000·2017-03-01

    New Flyer Transit Buses Recalled for Front Axle Beam Cracks

    New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.

    Product
    NEW FLYER — NEW FLYER GE40LF, D60LFR, D60LF, C35LF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1497-2017·2017-03-01

    Palmer's Candies Cookies & Cream Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Cookies & Cream Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Cookies & Cream Bark, NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC Code 77232-17254
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0475-2017·2017-03-01

    Apotex Recalls Cyclosporine Capsules Due to Impurity Failures

    Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.

    Product
    CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V131000·2017-03-01

    REV Recalls 2017 Ambulances Due to Rear Brake Bolt Torque Issue

    REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.

    Product
    MARQUE — MARQUE, FRONTLINE, WHEELED COACH TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1165-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Trial Trays Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1498-2017·2017-03-01

    Palmer's Candies Creme De Menthe Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Creme De Menthe Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g) packaged in cardboard boxes, UPC Code 77232-16043, B) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPS code 77232-17255; C) NET WT 10 lbs Net Weight (4.54 kg) packaged in cardboard boxes
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1502-2017·2017-03-01

    Palmer's Candies Peppermint Bark Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling Peppermint Bark candy because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232-23091; C) NET WT 8 OZ (226 g) packaged in paper boxes UPC 77232-12146; C) NET WT 9 OZ (255 g)…
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1505-2017·2017-03-01

    Palmer Candy Recalls Trail's End Chocolatey Crunch Due to Salmonella Risk

    Palmer Candy Co is recalling Trail's End Gourmet Chocolatey Crunch because an ingredient may be contaminated with Salmonella.

    Product
    Trail's End Gourmet Chocolatey Crunch A) NET WT 18 OZ (1.13 LB) 510 g, packaged in foil bags; B) NET WT 15 OZ packaged in foil bags;
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1510-2017·2017-03-01

    Palmer's Chocolatey Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10798
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-1167-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Devices)·Z-1164-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Drugs)·D-0480-2017·2017-03-01

    Hospira Recalls Metronidazole Injection Bags Due to Leaking

    Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.

    Product
    METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1526-2017·2017-03-01

    Golden Flake Potato Chips Recalled for Undeclared Milk

    Golden Flake is recalling Hot Thin & Crispy Potato Chips due to undeclared milk, a major allergen. The recall covers 14 states.

    Product
    Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL 35201, UPC 0-72080-00240-3
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-1161-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1172-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Material Inclusions

    Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1225-2017·2017-03-01

    Tosoh HLC-723G8 Analyzer Recalled for HbA1c Test Inaccuracy

    Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.

    Product
    Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-1174-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1157-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states