The Recall Desk

State

South Carolina product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41976–42000 of 80962

  • SevereFDA (Food)·F-1603-2018·2018-07-04

    Utz Recalls Tortilla Chips for Undeclared Milk Allergen

    Utz Quality Foods is voluntarily recalling select tortilla chip items due to potential contamination with undeclared milk allergen.

    Product
    Good Health Organic Tortillas; Black Bean & Rice; Net Wt 5.5 oz; Distributed by Good Health Natural Products, Inc. Greensboro, NC; UPC: 274077-55355-04100-9; Exp date: DEC 29 18; Mexico only: Good Health Totopos Organicos; Frijol Negro y Arroz; Cont. Neto 538,6 g…
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2281-2018·2018-07-04

    Konica Minolta CS-7 Medical Device Recall Due to Laptop Fire Risk

    Konica Minolta is recalling CS-7 medical devices because the Panasonic Toughbook laptops used in some configurations have a potential battery ignition risk.

    Product
    CS-7, Model No. A4C1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1598-2018·2018-07-04

    Utz and Weis Tortilla Chips Recalled for Undeclared Milk Allergen

    Utz Quality Foods is voluntarily recalling select tortilla chip products due to potential contamination with undeclared milk allergen.

    Product
    Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16 18; UTZ Quality Foods, Inc., Hanover, PA 17331; Utz Restaurant Style Tortilla Chips; Net Wt 11.5 oz; White Corn Tortilla Chips; UPC: 0-41780-00384-3; Exp…
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1602-2018·2018-07-04

    Utz Recalls Golden Flake Tortilla Chips for Undeclared Milk Allergen

    Utz Quality Foods is voluntarily recalling select Golden Flake tortilla chips due to potential contamination with undeclared milk allergen.

    Product
    Golden Flake TORTIYAHS! Superior Dipping Chips; Net Wt 12.5 oz Tortilla Chips; Golden Flake Snack Foods, Inc. Birmingham, AL 35201; UPC: 0-72080-41000-0; Exp date: JUN 2 18 to JUN 23 18;
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1601-2018·2018-07-04

    Utz Recalls Tortilla Chips Due to Undeclared Milk Allergen

    Utz Quality Foods is voluntarily recalling select tortilla chip items due to potential contamination with undeclared milk allergen.

    Product
    Weis Signature Collection No Salt Added White Corn Tortilla Chips; Net Wt 11 oz; Manufactured For Weis Markets, Sunbury, PA 17801; UPC: 0-41497-00427-0; Exp date: May 26 18 to JUN 16 18;
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2300-2018·2018-07-04

    Philips OmniDiagnost-Eleva X-ray System Recalled Due to Table Rotation Hazard

    Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.

    Product
    OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2323-2018·2018-07-04

    St Jude Medical Recalls Promote Quadra ICDs for Security Firmware Update

    St Jude Medical is recalling Promote Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2320-2018·2018-07-04

    St Jude Medical Recalls Fortify ICDs and CRT-Ds for Security Firmware Update

    St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.

    Product
    Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2287-2018·2018-07-04

    Teleflex Universal Shears Recalled Due to Handle Melting During Sterilization

    Teleflex Medical Europe Ltd is recalling 573 units of Pilling Universal Shears because incorrect plastic was used for the handles, causing them to melt during sterilization.

    Product
    Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2317-2018·2018-07-04

    Medtronic Model 53401 Pacemakers Recalled for Unexpected Power Reset

    Medtronic is recalling 1,108 Model 53401 temporary external pacemakers because they may revert to nominal settings during use due to an unexpected power on reset.

    Product
    Single Chamber Temporary External Pacemaker, Model 53401
    Category
    Medical Device
    Distribution
    45 states
  • HighFDA (Devices)·Z-2313-2018·2018-07-04

    Siemens Artis zee MP Recall for Display Failure After Power Save

    Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.

    Product
    Artis zee MP, Material no. 10094139, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2322-2018·2018-07-04

    St Jude Medical Recalls High Voltage Implantable Cardiac Devices for Security Firmware

    St Jude Medical is releasing new firmware for high voltage implantable cardiac devices to strengthen security against unauthorized access.

    Product
    Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2305-2018·2018-07-04

    Siemens Artis Q.zen Biplane Recalled for Display Failure

    Siemens Medical Solutions is recalling two Artis Q.zen biplane systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation or patient transfer.

    Product
    Artis Q.zen biplane, Material no. 10848355, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2304-2018·2018-07-04

    Siemens Artis Q Ceiling Recalled for Display Failure After Power Save

    Siemens Medical Solutions is recalling five Artis Q ceiling units because the display may fail to show an image after exiting power save mode, potentially requiring treatment cancellation.

    Product
    Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2314-2018·2018-07-04

    Siemens Artis zeego X-ray System Recalled for Display Failure

    Siemens Medical Solutions is recalling 56 Artis zeego systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.

    Product
    Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2308-2018·2018-07-04

    Siemens Artis zee Biplane Recalled for Display Failure After Power Save

    Siemens is recalling 68 Artis zee biplane systems because the large display may remain black after exiting power save mode, potentially requiring treatment cancellation or patient transfer.

    Product
    Artis zee biplane, Material no. 10094141, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2288-2018·2018-07-04

    HLD Systems Washer Pasteurizer Recalled for Terminal Block Overheating

    Cenorin, LLC is recalling 14 HLD Systems 600 Series Washer/Pasteurizers because a supplier quality issue with terminal blocks may cause overheating, charring, or burning.

    Product
    HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model 610HT, 230V Product Usage: Clean and thermally disinfect medical devices using full immersion pasteurization
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2327-2018·2018-07-04

    St Jude Medical Recalls Unify Assura ICDs for Security Firmware Update

    St Jude Medical is recalling Unify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Unify Assura, Sterile EO, Model #/ Part #: CD3257-40/100042333, 100059944; CD3257-40Q/100042334, 100059936; CD3261-40/100048460, 100048546, 100059897, 100059954, 100059996, 100078828; CD3261-40Q/100048568, 100048581, 100059898, 100059955, 100059997, 100078853…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2325-2018·2018-07-04

    St Jude Medical Recalls Quadra Assura MP Implantable Cardiac Devices for Security Update

    St Jude Medical is recalling 68,117 Quadra Assura MP implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Quadra Assura MP, Sterile EO, Model #/ Part #: CD3269-40/100043177; CD3269-40Q/100043178; CD3271-40/100043130; CD3271-40Q/100043191; CD3369-40C/100080339, 100080478; CD3369-40Q/100080439, 100080476, 100105528; CD3371-40/100078814, 100079232, 100079513…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2324-2018·2018-07-04

    St Jude Medical Recalls Quadra Assura ICDs for Security Firmware Update

    St Jude Medical is recalling 72,673 Quadra Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Quadra Assura, Sterile EO, Model #/ Part #: CD3265-40/100042335, 100059846; CD3265-40Q/100042336, 100059847; CD3267-40/100042956, 100043569, 100059961, 100078810; CD3267-40Q/100043132, 100043539, 100059917, 100059956, 100078904; CD3365-40C/100080435, 100080436…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2328-2018·2018-07-04

    St Jude Medical Recalls Unify Quadra ICDs for Security Firmware Update

    St Jude Medical is recalling Unify Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2312-2018·2018-07-04

    Siemens Artis zee floor MN recalled for display failure

    Siemens is recalling Artis zee floor MN systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.

    Product
    Artis zee floor MN, Material no. 10094142, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2290-2018·2018-07-04

    RayStation Radiation Therapy Software Recalled for Dose Calculation Accuracy Issues

    RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software versions 6.0 through 7.0 because dose calculation accuracy may be less than expected in some situations.

    Product
    RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2318-2018·2018-07-04

    St Jude Medical Recalls Implantable Cardiac Devices for Security Firmware Update

    St Jude Medical is recalling implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407…
    Category
    Medical Device
    Distribution
    Distributed nationwide