The Recall Desk

State

South Carolina product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39626–39650 of 80959

  • SevereFDA (Drugs)·D-0267-2019·2018-11-28

    Sciegen Recalls Irbesartan Tablets Due to NDEA Impurity

    Sciegen Pharmaceuticals is recalling Westminister Irbesartan Tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).

    Product
    Westminister Irbesartan Tablets, USP, 75 mg (a) 30-count bottle (NDC 69367-119-01), (b) 90-count bottle (NDC 69367-119-03), Rx Only, Manufactured by ScieGen Pharmaceuticals Inc Hauppauge, NY 11755 Manufactured for Westminister Pharmaceuticals LLC Olive Branch, MS 20854 Made in…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V843000·2018-11-28

    Keystone RV Recalls 2019 Travel Trailers Due to Axle Hub Bearing Defect

    Keystone RV Company is recalling certain 2019 recreational trailers because the inner axle hub bearings may not have been sufficiently greased, which could cause overheating, hub failure, and increased crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN OUTBACK, BULLET, AEROLITE, COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V846000·2018-11-28

    Blue Bird Recalls School Buses Due to Seat Detachment Risk

    Blue Bird is recalling certain 2019-2020 school buses because seats may detach from the floor in a crash, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2019·2018-11-28

    Sciegen Pharmaceuticals Recalls Irbesartan Tablets Due to NDEA Impurity

    Sciegen Pharmaceuticals is recalling Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).

    Product
    Westminister Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 69367-120-01), (b) 90-count bottle (NDC 69367-120-03), Rx Only, Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755, Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854, Made…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0474-2019·2018-11-28

    Boston Scientific Recalls SQ-RX Pulse Generators for Battery Malfunctions

    Boston Scientific is recalling 12,900 SQ-RX Pulse Generators used in S-ICD systems due to latent internal battery malfunctions that cause accelerated depletion.

    Product
    The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The S-ICD System is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V848000·2018-11-28

    Honda Recalls 2019 Ridgeline and Pilot for Air Bag Deployment Risk

    Honda is recalling 2019 Ridgeline and Pilot vehicles because a trim panel clip may interfere with right-side curtain air bag deployment in a crash.

    Product
    HONDA — HONDA PILOT, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0475-2019·2018-11-28

    Tosoh AIA-2000 Analyzer Recall Due to Potential Wash Solution Defect

    Tosoh Bioscience is recalling seven AIA-2000 analyzers because a liquid suction pump defect may cause incomplete washing, leading to inaccurate test results.

    Product
    AIA-2000 Analyzer, Model Nos. AIA-2000LA, AIA-2000ST - Product Usage: The AIA-2000 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric immunoassay. An…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0482-2019·2018-11-28

    GE Healthcare Recalls Panda iRes Infant Radiant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda iRes Infant Radiant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda iRes Infant Radiant Warmer. Device sold under the following product names: Panda iRes Warmer and Panda iRes Bedded Warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2019·2018-11-28

    GE Healthcare Recalls Panda Freestanding Infant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda Freestanding Infant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda Freestanding Warmer. Device sold under the following product names: Panda Freestanding Warmer and Panda Freestanding Warmer Generic ATO Model. Infant Radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V844000·2018-11-28

    Porsche Recalls 2017-2018 Models Due to Ski Bag Strap Defect

    Porsche is recalling certain 2017-2018 Cayenne and Macan vehicles because the optional ski bag strap may tear, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYENNE, MACAN, MACAN GTS, MACAN S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0266-2019·2018-11-28

    L. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles

    L. Perrigo is recalling specific lots of calcium carbonate antacid tablets because they were found to contain metal particles.

    Product
    Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2019·2018-11-28

    GE Healthcare Recalls Giraffe Infant Warmers Due to Electric Leakage Risk

    GE Healthcare is recalling 1,724 Giraffe infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2019·2018-11-28

    GE Healthcare Recalls Giraffe Incubator Carestations Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe Incubator Carestations worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0479-2019·2018-11-28

    GE Healthcare Recalls Giraffe OmniBed Neonatal Incubators Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe OmniBed Carestation neonatal incubators worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0489-2019·2018-11-28

    Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues

    Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.

    Product
    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2019·2018-11-28

    Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.

    Product
    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0283-2019·2018-11-28

    Dr. Reddy's Recalls Clopidogrel Tablets Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling specific lots of Clopidogrel Bisulfate tablets because they failed dissolution testing during stability checks.

    Product
    CLOPIDOGREL BISULFATE — CLOPIDOGREL BISULFATE (CLOPIDOGREL BISULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0275-2019·2018-11-28

    Ecolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error

    Ecolab Inc is recalling 14,108 bottles of Medi-Stat Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.

    Product
    Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2019·2018-11-28

    GE Healthcare Recalls DeltaVision OMX SR Imaging Systems Due to Interlock Defect

    GE Healthcare Biosciences is recalling 39 DeltaVision OMX SR Imaging Systems because the safety interlocks are not wired to be single-fault tolerant.

    Product
    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0273-2019·2018-11-28

    Nitrofurantoin Capsules Recalled for Potential Cross-Contamination with Unrelated Ingredients

    American Health Packaging is recalling specific lots of Nitrofurantoin Capsules due to potential cross-contamination with unrelated active ingredients.

    Product
    Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V836000·2018-11-27

    Audi Recalls A5 and A4 Allroad for Passenger Air Bag Defect

    Volkswagen Group of America is recalling 2018 Audi A5 Sportback and 2017-2018 Audi A4 Allroad vehicles because a passenger air bag mounting screw may not be sufficiently tightened.

    Product
    AUDI — AUDI A5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide