The Recall Desk

State

South Carolina product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31501–31525 of 80889

  • ModerateFDA (Devices)·Z-2337-2020·2020-06-17

    Philips SureSigns VM1 Monitor Recalled Due to Unverified Manufacturing Records

    Philips is recalling a specific SureSigns VM1 patient monitor because it was not intended for commercial distribution and lacks manufacturing records.

    Product
    Philips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 is a patient monitor that measures oxygen saturation (Sp02), respiration and CO2. The user interface is designed for fast and intuitive operation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2317-2020·2020-06-17

    Biomet Recalls Proximal Humerus Plating System Due to Design History Deficiencies

    Biomet is recalling the A.L.P.S. Proximal Humerus Plating System because it was distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 11 HOLE 190MM, Item Number: 110030208 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2360-2020·2020-06-17

    Physio-Control Recalls Infant Child Starter Kits Due to Packaging Seal Issues

    Physio-Control is recalling 6,732 Infant Child Starter Kits because the packaging for the reduced energy electrodes was not properly sealed.

    Product
    Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibrillation Electrodes, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2321-2020·2020-06-17

    Biomet Recalls A.L.P.S. Proximal Humerus Plating System for Design Documentation Issues

    Biomet is recalling A.L.P.S. Proximal Humerus Plating System plates because they were distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 14 HOLE 234MM, Item Number: 110030309 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2320-2020·2020-06-17

    Biomet A.L.P.S. Proximal Humerus Plating System Recalled for Design History Deficiencies

    Biomet is recalling A.L.P.S. Proximal Humerus Plating System units because they were distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM, Item Number: 110030308 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2311-2020·2020-06-17

    Biomet A.L.P.S. Proximal Humerus Plating System Locking Pegs Recalled

    Biomet is recalling A.L.P.S. Proximal Humerus Plating System 3.2mm Locking Pegs 60mm because they were distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 60MM , Item Number: 110025460 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2359-2020·2020-06-17

    Physio-Control Recalls Infant Defibrillation Electrodes Due to Packaging Seal Issues

    Physio-Control is recalling infant and child defibrillation electrodes because the packaging was not properly sealed. The recall affects units manufactured between August 2017 and October 2019.

    Product
    Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel who are trained on the device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2318-2020·2020-06-17

    Biomet A.L.P.S. Proximal Humerus Plating System Recalled for Design Documentation Deficiencies

    Biomet is recalling A.L.P.S. Proximal Humerus Plating System units distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 14 HOLE 227MM, Item Number: 110030209 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1340-2020·2020-06-17

    Akorn Recalls Prednisolone Sodium Phosphate Oral Solution Due to Discoloration

    Akorn, Inc. is recalling specific lots of Prednisolone Sodium Phosphate Oral Solution because the product failed a color test.

    Product
    Prednisolone Sodium Phosphate Oral Solution, 5 mg/5 mL, 120 mL Bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-040-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20V358000·2020-06-16

    Recreational vehicles with incorrect automatic parking function manual

    Forest River, Coachmen, and Dynamax recreational vehicles have an Operator's Manual that incorrectly describes the automatic parking function, potentially causing drivers to rely on it incorrectly and risking vehicle rollaway or movement.

    Product
    DYNAMAX — DYNAMAX, FOREST RIVER, COACHMEN ISATA, SUNSEEKER, BATTISTI, PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V357000·2020-06-15

    Blue Bird Recalls 2020 Vision Buses Due to Steering Drag Link Issue

    Blue Bird is recalling 2020 Vision buses because steering drag link connections may not be tightened correctly, potentially causing loss of steering control.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V355000·2020-06-15

    BMW and Toyota Recall Vehicles for Steering Tie Rod Fracture Risk

    BMW and Toyota are recalling specific 2019-2020 models because a steering tie rod may fracture, increasing crash risk. Dealers will replace the parts free of charge.

    Product
    BMW — BMW, TOYOTA X4, 330I, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V356000·2020-06-15

    Blue Bird Recalls 2019-2021 Vision School Buses for Steering Defect

    Blue Bird is recalling 2019-2021 Vision school buses because steering drag link connections may not be tightened, risking loss of control.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E039000·2020-06-15

    Lippert 3000 Series Frameless RV Windows Recalled for Adhesive Failure

    Lippert Components is recalling 3000 Series Frameless windows for recreational vehicles because the adhesive bond may fail, allowing glass to detach and become a projectile.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V353000·2020-06-15

    Spartan Fire Gladiator Recall for Wireless Remote Controller Battery Issue

    Spartan Fire is recalling one 2019 Gladiator firefighting vehicle because a disabled sleep mode on the wireless remote controller causes batteries to discharge faster than normal.

    Product
    SPARTAN FIRE — SPARTAN FIRE GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·012-2020·2020-06-13

    Lakeside Refrigerated Services Recalls Ground Beef Due to E. coli O157:H7 Risk

    Lakeside Refrigerated Services is recalling approximately 42,922 pounds of ground beef products that may be contaminated with E. coli O157:H7.

    Product
    Lakeside Refrigerated Services — Lakeside Refrigerated Services Recalls Beef Products due to Possible E.coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V347000·2020-06-12

    Mazda Recalls 2020 CX-30 AWD Vehicles for Fuel Leak Risk

    Mazda is recalling 2020 CX-30 all-wheel drive vehicles because a disconnected fuel hose may leak, increasing fire and crash risks.

    Product
    MAZDA — MAZDA CX-30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V346000·2020-06-12

    Mazda Recalls 2020 Mazda3 and CX-30 for Brake Caliper Bolt Issue

    Mazda is recalling 2020 Mazda3 and CX-30 vehicles because front brake caliper mounting bolts may not have been tightened properly, which could reduce braking performance.

    Product
    MAZDA — MAZDA MAZDA3, CX-30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V352000·2020-06-12

    MCI Recalls 2018-2020 Buses Due to Alternator Voltage Issue

    Motor Coach Industries is recalling 1,067 buses because debris or water may cause excessive alternator voltage, leading to engine shutdown and increased crash risk.

    Product
    MCI — MCI J4500, D45 CRT LE, D4005, D4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V351000·2020-06-12

    Keystone Recalls 2020 Trailers Due to Window Glass Detachment Risk

    Keystone RV Company is recalling 428 model-year 2020 trailers because window glass may detach while moving, creating a projectile hazard.

    Product
    KEYSTONE — KEYSTONE, CROSSROADS, DUTCHMEN RAPTOR, REDWOOD, VOLTAGE, ALPINE
    Category
    Vehicle
    Distribution
    Distributed nationwide