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.

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.

33901–33925 of 80890

  • ModerateFDA (Devices)·Z-0631-2020·2019-12-18

    Integra C7000 CUSA Clarity System Recalled for Sterilization Drying Defect

    Integra LifeSciences is recalling 820 C7000 CUSA Clarity systems because the 36 kHz sterilization tray requires 40 minutes to dry, not the 30 minutes stated in the manual.

    Product
    C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Drugs)·D-0597-2020·2019-12-18

    Anazao Health Recalls Clonidine, Baclofen, and Fentanyl Citrate Due to Fungal Contamination

    Anazao Health is recalling Clonidine HCL, Baclofen, and Fentanyl Citrate products due to the detection of Talaromyces rotundus fungi.

    Product
    Clonidine HCL and Baclofen and Fentanyl Citrate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0613-2020·2019-12-18

    Integra C7000 CUSA Clarity System Recalled for Inadequate Sterilization Tray Drying

    Integra LifeSciences is recalling 820 C7000 CUSA Clarity Ultrasonic Tissue Ablation Systems because the 36 kHz Sterilization Tray does not meet the 30-minute drying time criteria stated in the manual.

    Product
    C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0640-2020·2019-12-18

    Integra C7000 CUSA Clarity System Recall for Sterilization Tray Drying Defect

    Integra LifeSciences is recalling the C7000 CUSA Clarity System because the 36 kHz Sterilization Tray requires 40 minutes to dry, not the 30 minutes stated in the manual.

    Product
    C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0654-2020·2019-12-18

    Integra C7000 CUSA Clarity System Recalled for Inadequate Drying Time

    Integra LifeSciences is recalling the C7000 CUSA Clarity System because the 36 kHz Sterilization Tray does not meet the 30-minute drying criteria stated in the manual.

    Product
    C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0657-2020·2019-12-18

    Medtronic Passive Biopsy Needle Kit Recall for Depth Stop Issue

    Medtronic is recalling 10,448 Passive Biopsy Needle Kits because a manufacturing issue may cause depth stops to fail, potentially delaying surgery.

    Product
    Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-0625-2020·2019-12-18

    Integra CUSA Clarity System Recalled for Inadequate Sterilization Tray Drying Time

    Integra LifeSciences is recalling 820 CUSA Clarity Ultrasonic Tissue Ablation Systems because the 36 kHz Sterilization Tray requires 40 minutes to dry, not the 30 minutes stated in the manual.

    Product
    C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0674-2020·2019-12-18

    Volcano FFR Software Recalled for Interoperability Issues with Hemodynamic Systems

    Volcano Corporation is recalling FFR software due to interoperability issues when connected to specific Hemodynamic Systems.

    Product
    Philips Volcano FFR software used in the following systems connected to the McKesson, Schwarzer, and some Philips Xper Hemodynamic Systems (HMS): (1) Volcano Imaging System s5i, Part #807400001; (2) s5ix Imaging System with s5iz PC Workstation Refurbished, Part#807400001 R and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0661-2020·2019-12-18

    Young Dental Recalls Oral-B Fluoride Varnish Due to Shelf Life Labeling

    Young Dental Manufacturing Co, LLC is recalling Oral-B 5% Sodium Fluoride Varnish because the product shelf life may be shorter than indicated on the label.

    Product
    Oral-B, Practitioner Series, 5% Sodium Fluoride Varnish, 500 units (40mL/each) - Product Usage: For dentinal hypersensitivity and for the reduction of post-operative sensitivity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V897000·2019-12-17

    Oliver Travel Trailers Recalls Elite II Models Due to Axle Bolt Issues

    Oliver Travel Trailers is recalling 2017-2019 Elite II travel trailers because improperly tightened axle bolts may affect braking or cause wheel detachment.

    Product
    OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V900000·2019-12-17

    Prevost Recalls 2020 Coach Buses Due to Driveshaft Bolt Tightening Issue

    Prevost is recalling 2020 X3-45 and H3-45 coach buses because driveshaft clamp bolts may not be properly tightened, which could cause loss of drive or a road hazard.

    Product
    PREVOST — PREVOST X3-45, H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20040·2019-12-17

    J. Crew Recalls Boys' Denim Pants Due to Choking Hazards

    J. Crew is recalling specific boys' denim pants because small stones from the manufacturing process may remain in the pockets or waistband, posing a choking risk to young children.

    Product
    Crewcuts boys' stone washed denim pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V893000·2019-12-16

    Foretravel Recalls 2020 Realm and iH45 Vehicles Due to Brake Defect

    Foretravel is recalling 2020 Realm and iH45 vehicles because a brake relay valve defect may increase stopping distance, raising crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM, IH-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V896000·2019-12-16

    Mack Trucks Recalls 2020 Models for Steering Drag Link Defect

    Mack Trucks is recalling 2020 Anthem, Granite, and Pinnacle vehicles because steering drag link connections may be improperly installed, risking loss of steering control.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (CHU), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V894000·2019-12-16

    Maintainer Recalls 2019 Custom Body Heavy Rescue Vehicle for Shock Defect

    Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because front shocks may separate, potentially causing a steering fluid leak and loss of power steering assist.

    Product
    MAINTAINER — MAINTAINER CUSTOM BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V892000·2019-12-16

    Mercedes-Benz Recalls CLA Models Due to Air Bag Calibration Issue

    Mercedes-Benz is recalling certain 2015-2018 CLA models because the passenger air bag may not deploy properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLA 250, CLA250, AMG CLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V891000·2019-12-13

    Forest River Recalls 2020 Motorhomes Due to Trailer Hitch Bolt Issue

    Forest River is recalling 2020 Georgetown and FR3 motorhomes because trailer hitch bolts may not be properly tightened, posing a crash risk while towing.

    Product
    FOREST RIVER — FOREST RIVER FR3, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-121319·2019-12-13

    USDA Issues Public Health Alert for H-E-B Butter Chicken Soup

    USDA FSIS issued a public health alert for H-E-B Butter Chicken Soup due to undeclared wheat and soy allergens.

    Product
    FSIS Issues Public Health Alert for Chicken Soup due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V885000·2019-12-12

    Chrysler Recalls 2005-2006 Dodge Viper for Airbag Deployment Defect

    Chrysler is recalling 2005-2006 Dodge Viper vehicles because the Occupant Restraint Control module may inadvertently deploy air bags and seat belt pretensioners, increasing injury risk.

    Product
    DODGE — DODGE VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V890000·2019-12-12

    Maintainer Recalls 2019 Custom Body Heavy Rescue Vehicle for Brake Defect

    Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because a brake relay valve defect may cause extended stopping distances, increasing crash risk.

    Product
    MAINTAINER — MAINTAINER CUSTOM BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V888000·2019-12-12

    GM Recalls 2019-2020 Silverado and Sierra Trucks for Electrical Fire Risk

    General Motors is recalling 2019-2020 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because excessive glue on the battery cable may cause electrical arcing, stalling, or fire.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide