The Recall Desk

State

South Carolina product recalls

73,738 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.

Which agencies issued them

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33526–33550 of 80890

  • HighFDA (Devices)·Z-0802-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.

    Product
    BriteBlade Pro Single-se Fiber Optic Miller 2, CE 0120, Do not Re-use, Rx Only, REF, 040-722U, Sterile EO, Qty 10, (01) 15055788722783 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords and the glottis by insertion into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0808-2020·2020-01-22

    St. Jude Medical Recalls Confirm Rx Insertable Cardiac Monitors

    St. Jude Medical is recalling 2,906 Confirm Rx Insertable Cardiac Monitors because a software defect caused inappropriate low battery indicators.

    Product
    Merlin PCS Programmer software model 3330, used with Confirm Rx Insertable Cardiac Monitor (ICM), Model DM3500, Sterile. The firm name on the label of the ICM is St. Jude Medical Cardiac Rhythm Management Division, Sylmar, CA. - Product Usage: The Confirm Rx insertable cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0804-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal components may become loose and separate, posing a risk of entering the patient's oral cavity.

    Product
    BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI: (01)15055788724053(17)230901(10)181002320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0815-2020·2020-01-22

    Cook Inc. Recalls Dawson-Mueller Drainage Catheters Due to Leakage Risk

    Cook Inc. is recalling specific lots of Dawson-Mueller Drainage Catheters because they were not manufactured to specification, which could lead to leakage from the Mac-Loc hub assembly.

    Product
    Dawson-Mueller Drainage Catheter, Multipurpose Drainage Catheter, RPN UL T6.3-35-15-P-5S-CLDM-HC, UL T6. 3-35-25-P-58-CLDM-HC, UL T7.0-35-25-P-5S-CLDM-HC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0803-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.

    Product
    BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)15055788724138(17)230801(10)180900072 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0816-2020·2020-01-22

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillators Due to Keypad Oxidation

    Physio-Control is recalling 29,952 LIFEPAK 15 Monitor/Defibrillators worldwide because oxidation on the keypad may prevent the device from delivering a shock.

    Product
    LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0773-2020·2020-01-22

    Assurance Infusion Recalls TRIMIX Injection Vials Due to Sterility Concerns

    Assurance Infusion is recalling 1,290 vials of TRIMIX injection nationwide due to a lack of sterility assurance. No specific illnesses or injuries are reported in the source text.

    Product
    TRIMIX 30MG/1MG/10MCG/ML INJ in 5 mL/10 mL vials Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0802-2020·2020-01-22

    McGuff Compounding Pharmacy Recalls Lipoic Acid Injection Due to Particulate Matter

    McGuff Compounding Pharmacy Services is recalling Lipoic Acid Injection vials because filmy or cloudy particulate matter was observed in the product.

    Product
    Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid), 1,200 mg/30 mL (40 mg/mL) Sterile 30 mL Multiple Dose Vial, Rx Only, McGuff Compounding Pharmacy Services, Inc., Santa Ana, CA 92704
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0812-2020·2020-01-22

    Microbiologics Gram-Positive Blood Culture Control Panel Recall for Hydration Fluid Change

    Microbiologics Inc is recalling 810 units of the Gram-Positive Blood Culture Control Panel because the recommended hydration fluid has changed to sterile DI water or pH 7.2 phosphate buffer.

    Product
    Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used in test systems to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0805-2020·2020-01-22

    Caire FreeStyle Comfort Oxygen Concentrators Recalled for Lack of US Clearance

    Caire, Inc. is recalling four European version FreeStyle Comfort Oxygen Concentrators because they were not cleared for use in the US.

    Product
    CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The FreeStyle Comfort Oxygen Concentrator is intended for the administration of supplemental oxygen. The device is not intended for life support nor does it provide any patient monitoring capabilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0789-2020·2020-01-22

    AuroMedics Recalls Moxifloxacin Ophthalmic Solution Due to Discoloration

    AuroMedics Pharma LLC is recalling Moxifloxacin Ophthalmic Solution due to market complaints of discoloration. The affected product is distributed nationwide in the U.S.

    Product
    MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0790-2020·2020-01-22

    Lupin Recalls Tri-Lo-Marzia Tablets Due to Blend Uniformity Deviations

    Lupin Pharmaceuticals is recalling specific lots of Tri-Lo-Marzia oral contraceptives due to out-of-specification test results found during a retrospective review of blend uniformity data.

    Product
    Tri-Lo-Marzia (Norgestimate and Ethinyl Estradiol Tablets, USP), 0.180 mg/0.025 mg; 0.215mg/0.025 mg and 0.250 mg/0.025 mg, Pack size - 3 x 28's wallets/carton, Rx Only, Distributed by Lupin Pharmaceuticals, Inc, Baltimore MD 21202, Manufactured by: Lupin Limited, Pithampur…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V032000·2020-01-20

    Arcimoto Recalls 2019 FUV Motorcycles Due to Brake Line Wear Risk

    Arcimoto is recalling 2019 FUV motorcycles because the brake line may contact the steering main-link, potentially causing a loss of braking ability and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V023000·2020-01-17

    Terex Advance Mixer Recalls 2020 Concrete Mixers Due to Axle Shaft Fracture Risk

    Terex Advance Mixer is recalling 2020 FDC300, FD4000, FD5000GL, and FD7000B vehicles because incorrectly heat-treated axle output shafts may fracture, causing loss of drive and increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FDC300, FD5000GL, FD4000, FD7000B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V024000·2020-01-17

    Toyota Recalls Corolla, Matrix, Avalon Models for Air Bag Defect

    Toyota is recalling specific 2011-2019 Corolla, Matrix, Avalon, and Avalon Hybrid vehicles because the air bag control unit may malfunction, potentially preventing air bags and seat belt pretensioners from deploying in a crash.

    Product
    TOYOTA — TOYOTA AVALON, AVALON HYBRID, MATRIX, COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V026000·2020-01-17

    Honda, Acura, and Isuzu Recall Vehicles for Air Bag Inflator Defect

    Honda is recalling specific Acura, Honda, and Isuzu vehicles because driver air bag inflators may rupture or underinflate, posing a risk of injury.

    Product
    ISUZU — ISUZU, HONDA, ACURA OASIS, CIVIC, CR-V, EV PLUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V027000·2020-01-17

    Honda Recalls Vehicles for Driver Air Bag Inflator Rupture Risk

    Honda is recalling specific 2000-2003 Acura and Honda vehicles because replacement driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.

    Product
    ACURA — ACURA, HONDA MDX, CL, ODYSSEY, RL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V022000·2020-01-17

    Hyundai Recalls 2020 Kona Vehicles for Incorrect Weight Rating Label

    Hyundai is recalling 2020 Kona vehicles because the certification label may display an incorrect Gross Axle Weight Rating. Dealers will replace the label to ensure compliance with federal safety standards.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V025000·2020-01-17

    Isuzu and Chevrolet Trucks Recalled for Seat Belt Webbing Defect

    Isuzu and Chevrolet trucks are being recalled because a manufacturing issue may prevent the seat belt webbing locking mechanism from properly restraining occupants.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, NPR, NQR, NRR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V021000·2020-01-16

    Multiquip Recalls 2019 WT5C Trailers Due to Safety Chain Defect

    Multiquip is recalling 119 2019 WT5C trailers because incorrect safety chain attachment points may interfere with steering and increase crash risk.

    Product
    MULTIQUIP — MULTIQUIP WT5C
    Category
    Vehicle
    Distribution
    Distributed nationwide