The Recall Desk

State

South Carolina product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44926–44950 of 80970

  • ModerateFDA (Food)·F-0409-2018·2017-12-06

    Reese Pharmaceutical Recalls Orange Flavor Immune Support Effervescent Tablets

    Reese Pharmaceutical is recalling Orange Flavor Immune Support Effervescent Tablets because the label does not list sodium in the ingredient statement.

    Product
    Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Best Choice UPC 0 70038 60863 9 & UPC 0 70038 60863 9; Discount Drug Mart UPC 0 93351 00909 9; Freds Mart UPC 0 84579 12451 0; Good Neighbor…
    Category
    Food
    Distribution
    40 states
  • ModerateFDA (Devices)·Z-0180-2018·2017-12-06

    Arrow PICC Recall Due to Potential Incorrect Peel-Away Sheath Size

    Arrow International is recalling specific lots of ARROW PICC powered by ARROW VPS Stylet kits that may contain 5 Fr peel-away sheaths instead of the required 4 Fr.

    Product
    ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, power injection of contrast media and allows for central venous pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0098-2018·2017-12-06

    Mayne Pharma Recalls Liothyronine Sodium Tablets for Dissolution Failures

    Mayne Pharma Inc is recalling 11,364 bottles of Liothyronine Sodium Tablets 25 mcg because they failed dissolution specifications. The affected lot is distributed nationwide.

    Product
    Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC 0574-0222-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0188-2018·2017-12-06

    Medtronic Recalls Everflex Self-Expanding Peripheral Stents Due to Labeling Error

    Medtronic is recalling 21 units of Everflex Self-Expanding Peripheral Stents because the stent length on the label may not match the actual stent length.

    Product
    Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 140 mm in length in the native Superficial Femoral Artery (SFA) and/or proximal popliteal arteries…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·18047·2017-12-05

    Netgear Recalls Outdoor Camera Power Adapters Due to Fire Hazard

    Netgear is recalling VMA4700 power adapters for Arlo outdoor cameras because water leakage can cause short circuits, melting, and fire.

    Product
    Power adapters for outdoor Arlo cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18053·2017-12-05

    Metabo Recalls Rat Tail Angle Grinders Due to Laceration Hazard

    Metabo is recalling specific rat tail angle grinders because the on-off switch can lock in the on position, posing a laceration hazard.

    Product
    Rat tail angle grinders with brake
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V776000·2017-12-04

    Burch Recalls 1984 Evans Cargo Tank Trailers Due to Brake Caliper Bolts

    Burch Tank and Truck is recalling 1984 Evans Cargo Tank trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.

    Product
    EVANS — EVANS CARGO TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V778000·2017-12-04

    Triple E RV Recalls 2016-2018 Wonder Motorhomes for Seat Bolt Issue

    Triple E RV is recalling 2016-2018 Wonder motorhomes because improperly tightened passenger seat bolts may fail in a crash, increasing injury risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V777000·2017-12-04

    Temsa Recalls 2017-2018 Buses Due to Fire Suppression Chemical Contamination

    Temsa is recalling 2017-2018 TS30, TS35E, and TS45 buses because the fire suppression system may contain contaminated dry chemical, which could discharge improperly and increase injury risk.

    Product
    TEMSA — TEMSA TS45, TS30, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V775000·2017-12-01

    Ford Recalls 2018 Expedition Vehicles for Seat Back Bolt Defect

    Ford is recalling 2018 Expedition vehicles because second-row outboard seats may have improperly installed bolts or excessive forward adjustment, increasing injury risk in a crash.

    Product
    FORD — FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V772000·2017-12-01

    MV Agusta Recalls 2017 Brutale 800 Dragster RR for Rear Wheel Spokes

    MV Agusta is recalling 45 2017 Brutale 800 Dragster RR motorcycles because rear wheel spokes may loosen, potentially affecting handling and increasing crash risk.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18051·2017-12-01

    Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash Hazards

    Camso is recalling DTS 129 conversion kits because a brake pin can loosen, posing a crash or impact hazard. No injuries have been reported.

    Product
    Camso dirt to snow bike conversion kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V773000·2017-12-01

    Kia Recalls 2012-2014 Forte Models Due to Brake Pedal Stopper Pad Defect

    Kia is recalling 2012-2014 Forte and Forte Koup vehicles because a deteriorating brake pedal stopper pad may keep brake lights on or allow shifting without pressing the brake pedal.

    Product
    KIA — KIA FORTE KOUP, FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V769000·2017-11-30

    Hyundai Recalls 2013-2014 Elantra for Brake Pedal Stopper Pad Defect

    Hyundai is recalling 2013-2014 Elantra vehicles because a deteriorating brake pedal stopper pad can cause brake lights to stay on and allow shifting out of park without pressing the brake pedal.

    Product
    HYUNDAI — HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18049·2017-11-30

    Synodrin Pain Relieving Cream Recalled for Non-Child-Resistant Packaging

    Natural Solutions for Life is recalling Synodrin Pain Relieving Cream because the jar caps are not child-resistant, posing a poisoning risk to young children.

    Product
    Maximum Strength Synodrin Pain Relieving Cream with Lidocaine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18050·2017-11-30

    Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard

    Flos Inc. is recalling specific Romeo Moon and Romeo Louis II pendant light fixtures because the internal glass diffuser can detach and fall, posing an impact injury hazard.

    Product
    Pendant light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0167-2018·2017-11-29

    Zimmer Biomet ROSA Brain 3.0.0 Software Recall for Communication Errors

    Zimmer Biomet is recalling 18 units of ROSA Brain 3.0.0 software due to communication errors between software components and the controller.

    Product
    ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0072-2018·2017-11-29

    Spacelabs Arkon Anesthesia Workstation Recalled for Mechanical and Display Failures

    Spacelabs Healthcare is recalling 110 Arkon Anesthesia Workstations due to failures in ventilation, gas delivery, and display alarms.

    Product
    Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V768000·2017-11-29

    Ford Recalls 2017 F-53 and F-59 Chassis for Brake Fluid Leak Risk

    Ford is recalling 2017 F-53 and F-59 chassis because missing plugs in the brake control unit may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V766000·2017-11-29

    Volkswagen Recalls 2018 Atlas Vehicles Due to Fuel Tank Leak Risk

    Volkswagen is recalling 2018 Atlas vehicles because the fuel tank may have insufficient wall thickness, potentially causing a fuel leak and increasing fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0121-2018·2017-11-29

    Halyard Turbo-Cleaning Closed Suction System Saline Vials Recalled for Leaking Risk

    Halyard Health is recalling specific lots of 15ml saline vials used in the Turbo-Cleaning Closed Suction System because they may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, T-Piece, Wet Pak. 12 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states