The Recall Desk

State

South Carolina product recalls

73,741 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,152
Critical
1,275
Severe
2,169
Most recent
2026-10-28

Of the 7,152 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 2,169 (30%) are Severe.

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37376–37400 of 80893

  • ModerateFDA (Devices)·Z-1289-2019·2019-05-15

    Ortho-Clinical VITROS 3600 Immunoassay System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 3600 Immunoassay System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code: 6802783 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1300-2019·2019-05-15

    Siemens Atellica IM 1600 Analyzer Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 366 Atellica IM 1600 Analyzers due to multiple issues identified in the system software that required an update.

    Product
    Atellica IM 1600 Analyzer, Material Number 11066000
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Food)·F-1335-2019·2019-05-15

    Schreiber Foods Recalls Great Value Fiesta Blend Cheese Due to Plastic

    Schreiber Foods is recalling Great Value Fiesta Blend Cheese because it may contain hard plastic. The product was distributed to grocery stores in 30 states.

    Product
    Great Value, Finely Shredded, Fiesta Blend Cheese, Shredded Monterey Jack, Cheddar, Queso Quesadilla and Asadero Cheeses, Net Wt 8 oz; packaged in plastic pouches, 12 per case;
    Category
    Food
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-1288-2019·2019-05-15

    Ortho-Clinical VITROS 5600 Systems Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 5600 Integrated System Refurbished-Software V3.3.2 & below Product Code: 6802915 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1294-2019·2019-05-15

    Medica Wash1 Solution Recalled for Ineffective Probe Cleaning

    Medica Corporation is recalling Wash1 solution because it fails to clean the probe effectively, potentially causing test interference on the EasyRA analyzer.

    Product
    Medica Wash1-Wash solution used prior to Lipase assay on the EasyRA clinical chemistry analyzer REF 10680 - Product Usage: For use in washing the probe of the Medica EasyRA Chemistry Analyzer. The wash solution in the wedge is used to prevent interference between certain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1299-2019·2019-05-15

    Siemens Atellica IM 1300 Analyzer Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 277 Atellica IM 1300 Analyzers due to multiple issues identified in the system software that required an update.

    Product
    Atellica IM 1300 Analyzer, Material Number 11066001
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1291-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS XT 7600 Systems Due to Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 62 VITROS XT 7600 Integrated Systems worldwide because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code: 6844461 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1284-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Inconsistency

    Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.

    Product
    ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1293-2019·2019-05-15

    Ortho-Clinical VITROS ECi Immunodiagnostic System Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 25 refurbished VITROS ECi Immunodiagnostic Systems because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS ECi Immunodiagnostic System Refurbished Product Code: 6801059 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1297-2019·2019-05-15

    Elekta Unity Systems Recalled for Missing Contrast Agent Warnings

    Elekta Limited is recalling nine Elekta Unity systems because the user manual lacks a warning regarding the administration of unvalidated contrast agents.

    Product
    Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1292-2019·2019-05-15

    Ortho-Clinical VITROS ECi/ECiQ Immunodiagnostic System Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 45 VITROS ECi/ECiQ Immunodiagnostic Systems worldwide due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1290-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 3600 Immunoassay Systems Due to Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 28 VITROS 3600 Immunoassay Systems because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 3600 Immunoassay System Refurbished-Software V3.3.2 & below Product Code: 6802914 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 5600 Integrated System Software

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code: 6802413 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1334-2019·2019-05-15

    Schreiber Foods Recalls Colby and Monterey Jack Cheese for Foreign Material

    Schreiber Foods is recalling specific brands of Colby and Monterey Jack cheese due to the presence of hard plastic foreign material.

    Product
    Shredded and blocks of Colby & Monterey Jack cheese - Labeled and Packaged: 1) Great Value, Finely Shredded, Colby & Monterey Jack Cheese, Net Wt 8 oz; packaged in plastic pouches, 12 per case; 2) Great Value, Finely Shredded, Colby & Monterey Jack Cheese, Net Wt 16 oz…
    Category
    Food
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-1301-2019·2019-05-15

    Siemens Atellica Sample Handler Prime Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 474 Atellica Sample Handler Prime units due to multiple issues identified in the system software that required an update.

    Product
    Atellica Sample Handler Prime, Material Number 11069001
    Category
    Medical Device
    Distribution
    36 states
  • SevereNHTSA·19V367000·2019-05-14

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Brake Bolt Issue

    Daimler Trucks North America is recalling 253 specific 2019 heavy-duty trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing brake effectiveness.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR XCL, XCS, CASCADIA, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V368000·2019-05-14

    2019 Thomas Built Buses Saf-T-Liner C2 Brake Recall

    Daimler Trucks North America is recalling 2019 Thomas Built Buses Saf-T-Liner C2 vehicles because loose brake caliper bolts may reduce braking effectiveness.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V370000·2019-05-14

    Daimler Trucks Recalls 741 Vehicles for Insufficient Brake Air Reservoir Capacity

    Daimler Trucks North America is recalling 741 Freightliner, Sterling, and Western Star trucks because insufficient air reservoir capacity may reduce brake effectiveness and increase crash risk.

    Product
    STERLING — STERLING, FREIGHTLINER, WESTERN STAR ACTERRA, LT9500, L8500, CLASSIC XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V371000·2019-05-14

    Daimler Trucks Recalls MT55 and MT45 Chassis for Brake Pedal Defect

    Daimler Trucks North America is recalling 2012-2019 Freightliner Custom Chassis MT55 and MT45 vehicles because a brake pedal clip may detach, causing brake light failure or pedal detachment.

    Product
    FCCC — FCCC MT55, MT45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V363000·2019-05-14

    Mazda Recalls 2019 Mazda3 Vehicles for Incorrect Air Bag Indicator Light

    Mazda is recalling 2019 Mazda3 vehicles because the passenger air bag deactivation indicator light may turn off incorrectly, potentially leaving occupants unaware of safety system status.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V364000·2019-05-13

    LDJ Recalls 2019 Thunder Creek Trailers Due to Wheel Lug Nut Issues

    LDJ Manufacturing is recalling 102 2019 Thunder Creek trailers because wheel lug nuts may loosen, potentially causing a wheel to separate and increasing crash risk.

    Product
    THUNDER CREEK — THUNDER CREEK EV, SLT, MTT, FST
    Category
    Vehicle
    Distribution
    Distributed nationwide