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.

Which agencies issued them

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.

55726–55750 of 80986

  • ModerateFDA (Devices)·Z-0629-2016·2016-01-20

    Stryker Tourniquet Cuffs Recalled for Mislabeling Port Configuration

    Stryker is recalling 450 reprocessed tourniquet cuffs because they were mislabeled regarding their port configuration.

    Product
    Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135, 5921-034-135, 5921-034-235, 5921-024-236 Indicated for use in patients who require surgery of the extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0632-2016·2016-01-20

    Perkin Elmer WIZARD2 Gamma Counter Recall Due to Barcode Label Error

    Perkinelmer is recalling 47 WIZARD2 gamma counters because a barcode label error may cause the device to execute the wrong measurement protocol, potentially producing erroneous results.

    Product
    Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0628-2016·2016-01-20

    BD Biosciences Recalls FMC7 FITC Reagent Due to Functional Degradation

    Becton, Dickinson and Company is recalling FMC7 FITC reagents because functional degradation reduces the percent positive from 100% to approximately 87%.

    Product
    FMC7 FITC, Catalog No. 340918 Analyte Specific Reagent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0637-2016·2016-01-20

    Perkin Elmer WIZARD2 Gamma Counter Recalled for Barcode Label Error

    Perkinelmer is recalling 22 WIZARD2 gamma counters because a barcode label error may cause the device to execute the wrong measurement protocol, potentially producing erroneous results.

    Product
    Perkin Elmer WIZARD2 10-detector, 1000 samples. Product Code: 2470-0200, 3470-0200. The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0568-2016·2016-01-20

    Life-Line Docusate Calcium Stool Softener Recalled for Labeling Error

    National Vitamin Co Inc is recalling Life-Line Docusate Calcium stool softeners because they were mislabeled as Docusate Sodium.

    Product
    Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each, 100 softgels per bottle. UPC 0-79854-95005-2 Manufactured and Distributed by: NATIONAL VITAMIN COMPANY Casa Grande, AZ 85122. NDC 54629-0640-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0647-2016·2016-01-20

    Brainlab Brain Metastases Software Recall for Image Display Errors

    Brainlab AG is recalling Brain Metastases 1.0.0 software because large objects may display cropped during import.

    Product
    RT Elements are applications for radiation treatment planning for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions. The simulated plan is intended for treatment evaluation for example in tumor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0566-2016·2016-01-20

    Teva Recalls Amphetamine Tablets Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 9,717 bottles of mixed amphetamine salts tablets because stability testing revealed high impurity levels.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0638-2016·2016-01-20

    Perkin Elmer WIZARD2 Gamma Counter Recalled for Barcode Label Error

    Perkinelmer is recalling 188 WIZARD2 gamma counters because a barcode label error may cause the device to execute the wrong measurement protocol, potentially producing erroneous results.

    Product
    Perkin Elmer WIZARD2 1-detector,3", 1000 samples. Product Code: 2480-0010 The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V019000·2016-01-19

    Western Trailer Chip B-Train Recalled for Brake Drag Fire Risk

    Western Trailer is recalling 2015-2016 Chip B-Train trailers due to brake drag that may cause wheel end fires. Brake chambers have already been replaced.

    Product
    WESTERN TRAILER — WESTERN TRAILER CHIP B-TRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16077·2016-01-19

    West Elm Recalls Saddle Bar and Counter Stools Due to Fall Hazard

    West Elm is recalling Saddle bar and counter stools because the legs can break, posing a fall hazard. The firm received six reports of breaking, including one injury.

    Product
    Saddle bar and counter stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E002000·2016-01-19

    Mazda CX-5 Windshield Recall Due to Improperly Affixed Sensor Bracket

    Pilkington is recalling replacement windshields for Mazda CX-5 vehicles because the Smart City Brake Support sensor bracket may loosen, potentially disabling safety features.

    Product
    MAZDA — MAZDA CX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V018000·2016-01-19

    Suzuki Recalls Motorcycles Due to Electrical System Defect

    Suzuki is recalling certain 2008-2012 motorcycles because a faulty regulator/rectifier may cause the engine to stall while riding, increasing crash risk.

    Product
    SUZUKI — SUZUKI VLR1800, DL1000, GSX1300R, GSF1250S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·006-2016·2016-01-16

    Kayem Foods Recalls Chicken Sausage Due To Misbranding And Undeclared Pork

    Kayem Foods Inc. is recalling approximately 22,182 pounds of chicken sausage products due to incorrect nutritional labeling and undeclared pork casings.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Chicken Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V015000·2016-01-15

    Coachmen Cross Country Recalled for Fuel Guard Tire Damage Risk

    Forest River is recalling 2016 Coachmen Cross Country vehicles because the fuel fill guard may damage front tires, increasing crash risk.

    Product
    COACHMEN — COACHMEN CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V014000·2016-01-15

    Supreme Recalls Shuttle Buses Due to Wheelchair Lift Bearing Defect

    Supreme is recalling 2008-2014 shuttle buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.

    Product
    STARTRANS — STARTRANS CANDIDATE, SENTINEL BUS, AZURE HYBRID, PRESIDENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V012000·2016-01-14

    Eldorado Recalls 2010-2016 Buses Due to Seat Belt Anchor Weld Defect

    Eldorado is recalling specific 2010-2016 bus models because missing welds on seat brackets could cause seat belts to detach during a crash.

    Product
    ELDORADO — ELDORADO EZRM, XHF, AXESS, ARRIVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16074·2016-01-14

    Steelcase Recalls Rocky Swivel Chairs Due to Fall Hazard

    Steelcase is recalling about 17,000 Rocky model swivel chairs because screws can detach, posing a fall hazard. One injury was reported.

    Product
    Rocky model swivel chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16721·2016-01-14

    School Specialty Recalls NeoRok Stools Due to Fall Hazard

    School Specialty is expanding a recall of NeoRok stools that can break during use, posing a fall hazard to children.

    Product
    Classroom Select NeoRok Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide