The Recall Desk

State

South Carolina product recalls

19,789 recalls have nationwide distribution and so reach South Carolina. 0 additional recalls listed South Carolina specifically in their distribution scope.

About recalls in South Carolina

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect South Carolina consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

5826–5850 of 19789

  • HighNHTSA·24V442000·2025-02-06

    2023 Toyota Crown Rearview and Frontview Cameras May Separate

    Toyota is recalling certain 2023 Crown vehicles with defective rearview and frontview cameras that may separate and allow water infiltration, potentially failing to display images and reducing driver visibility.

    Product
    TOYOTA — 2023 TOYOTA CROWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V445000·2025-02-06

    Mercedes-Benz Fuel Pump May Fail, Causing Loss of Drive Power

    Mercedes-Benz USA is recalling certain 2021–2023 vehicles with faulty fuel pumps that may shutdown and cause loss of drive power. Owners should contact dealers for free replacement.

    Product
    MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V369000·2025-02-06

    2023 Mitsubishi Outlander: Rearview Camera Software Defect Recall

    Mitsubishi is recalling 198,940 certain 2022-2024 Outlander and 2023-2025 Outlander PHEV vehicles due to a software error that may freeze or prevent the rearview camera from displaying, reducing rear visibility and increasing crash risk.

    Product
    MITSUBISHI — 2023 MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25121·2025-02-06

    Bobcat and Steiner AirFX Finish Mower Deck Attachments Recalled for Crush Hazard

    Doosan Bobcat is recalling about 552 AirFX Finish Mower Deck attachments because the locking pins may fail to secure the deck during maintenance, creating a crush hazard. No injuries have been reported.

    Product
    Bobcat & Steiner AirFX Finish Mower Deck attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25123·2025-02-06

    Sling Carriers Recalled for Fall Hazard Due to Safety Violations

    About 18,650 sling carriers sold on Temu.com violate federal safety regulations for structural integrity and occupant retention, posing a fall hazard to babies. No injuries have been reported.

    Product
    Sling Carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V441000·2025-02-06

    Thor Motor Coach Motorcoaches: Emergency Exit Window Obstruction Recall

    Thor Motor Coach is recalling 2023-2024 Magnitude and Omni motorcoaches because the emergency exit window can become blocked when the outside griddle is in use, potentially delaying evacuation during an emergency.

    Product
    THOR MOTOR COACH — 2023 THOR MOTOR COACH MAGNITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V440000·2025-02-06

    2024 Ford Escape Adaptive Cruise Control Radar Misalignment

    Ford is recalling 2023-2024 Escape vehicles with adaptive cruise control due to misaligned radar modules. The misalignment can cause unexpected braking and loss of safety system function, increasing crash risk.

    Product
    FORD — 2024 FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25122·2025-02-06

    UVIPC Baby Gates Recalled for Entrapment Hazard Violation

    UVIPC Baby Gates sold on Amazon have been recalled due to an entrapment hazard that violates federal safety regulations, as children's torsos can fit through gaps in the gate design. No injuries have been reported.

    Product
    UVIPC Baby Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25120·2025-02-06

    Pella Sliding Patio Doors and Windows Recalled for Battery Ingestion Hazard

    Pella Corporation is recalling about 340 Pella Reserve and Lifestyle sliding patio doors and windows because their sensor panels and remote controls contain button cell batteries that children can easily access, posing an ingestion hazard.

    Product
    Pella Reserve and Lifestyle Sliding Patio Doors and Lifestyle Windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25124·2025-02-06

    Ariens Snow Throwers Recalled Due to Laceration Hazard from Continued Rotation

    Ariens snow throwers may continue rotating after the operator releases the control lever, creating a laceration hazard. The company is offering free repairs at authorized dealers.

    Product
    Ariens® DELUXE-, PLATINUM- and PROFESSIONAL-series Snow Throwers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25128·2025-02-06

    Roll-Up Window Blinds Recalled for Child Strangulation and Entanglement Hazards

    Thy Trading Company recalls approximately 720 roll-up window blinds sold on Wayfair.com due to long operating cords that pose strangulation and entanglement hazards to children. Consumers should stop using the blinds immediately and request a full refund.

    Product
    Roll Up Window Blinds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V446000·2025-02-06

    2022–2023 Porsche 911 GT3 Rear Spoiler Control Software Error

    A software error in the rear spoiler control unit may cause brake lights to activate simultaneously on 2022–2023 Porsche 911 GT3 vehicles, potentially confusing other drivers.

    Product
    PORSCHE — 2022 PORSCHE 911 GT3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0211-2025·2025-02-05

    Prograf Tacrolimus Capsules Recall: Empty Capsules in Bottles

    Astellas Pharma recalls Prograf (tacrolimus) 0.5 mg capsules distributed nationwide due to empty capsules in bottles. Affected lot 0E3353D expires March 31, 2026.

    Product
    PROGRAF — PROGRAF (TACROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0210-2025·2025-02-05

    FDA Class I Recall: Astagraf XL Immunosuppressant Capsules May Be Empty

    Astellas Pharma is recalling Astagraf XL (tacrolimus) due to manufacturing defects; bottles shipped nationwide may contain empty capsules instead of medication.

    Product
    ASTAGRAF XL — ASTAGRAF XL (TACROLIMUS EXTENDED-RELEASE CAPSULES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0991-2025·2025-02-05

    Medline Arterial Line Insertion Kits Recalled for Catheter Hub Defect

    Medline Industries is recalling 942 arterial line insertion kits due to excess material on the catheter hub of the catheter subassembly. The manufacturing defect prompted a FDA Class I recall of products distributed nationwide.

    Product
    Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERIAL LINE BUNDLE, Item Number ART255; 3) ARTERIAL LINE TRAY, Item Number ART350; 4) ARTERIAL LINE BUNDLE, Item Number ART355; 5) ARTERIAL LINE BUNDLE, Item Number ART355 ; 6)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0992-2025·2025-02-05

    Medline General Surgery Arterial Line Tray kits recalled for manufacturing defect

    Medline arterial line tray kits (models ART600 and ART690) are being recalled because the catheter hub contains excess material from manufacturing. The recall affects 58 kits distributed nationwide.

    Product
    Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0431-2025·2025-02-05

    Frozen peach mango sorbet recalled for undeclared egg allergen

    The Mochi Ice Cream Company is recalling My Mochi Sorbet Peach Mango Sorbet nationwide due to undeclared egg allergen. Consumers with egg allergies should not consume this product.

    Product
    My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES NET WT 7.5 OZ (210g)*** Nutritional Panel: 6 servings per container; JOYFULLY CHILL!; Made in a nut-free facility; Made by My/Mochi, 5563 Alcoa Ave., Los Angeles, CA 90058; www.mymochi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V335000·2025-02-05

    2025 Freightliner Business Class M2 park brake failure recall

    Daimler Trucks North America is recalling 2024-2025 Freightliner Business Class M2 vehicles because the park brake valve module may leak, causing park brake failure or unexpected engagement while driving.

    Product
    FREIGHTLINER — 2025 FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1069-2025·2025-02-05

    Bedside cardiac monitor system recalled for display distortion

    The muRata Vios Monitoring System Model 2050 bedside cardiac monitor has been recalled due to a software issue causing patient vital signs and ECG waveforms to flicker and become distorted on the Central Station Monitor. No injuries have been reported.

    Product
    muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V253000·2025-02-05

    Mercedes-Benz C 300 and AMG C 43 Seat Belt Cover Defect Recall

    Mercedes-Benz is recalling certain 2022-2025 C 300 and 2023-2024 AMG C 43 vehicles. The driver-side seat belt cover may not be properly installed, potentially causing the seat belt anchor to loosen.

    Product
    MERCEDES-BENZ — 2022 MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1051-2025·2025-02-05

    Karl Storz Uretero-Renoscope Recalled for Unapproved Reprocessing Instructions

    Karl Storz is recalling a uretero-renoscope surgical device (REF 27003L) because the reprocessing instructions in the product documentation have not been reviewed or approved by the FDA.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27003L, MICHEL Uretero-Renoscope, 9.5 Fr., 43cm, RxONLY, CE0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1041-2025·2025-02-05

    Medline procedure kits recalled for surgical masks failing sterilization tests

    Medline SHORT TERM INFUSAPORT ACCESS KIT with reorder number DYNDC3188 is recalled because included surgical masks failed bioburden testing, potentially compromising sterility during procedures.

    Product
    Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT, Reorder number DYNDC3188; surgery tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V380000·2025-02-05

    Ford Escape, Maverick, and Corsair Engine Fire Risk Recall

    Ford is recalling certain 2020-2023 Escape, 2022-2023 Maverick, and 2021-2023 Corsair vehicles due to a 2.5L engine defect that could cause an engine compartment fire. No injuries have been reported.

    Product
    FORD — 2020 FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2025·2025-02-05

    HemosIL Heparin Calibrators Recalled Over Quality Control Test Failures

    Instrumentation Laboratory recalls HemosIL Heparin Calibrators worldwide due to quality control failures. The diagnostic controls did not meet expected performance standards, potentially affecting accuracy of heparin testing in clinical laboratories.

    Product
    HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1060-2025·2025-02-05

    Karl Storz Ureteroscope Recall Due to Unapproved Reprocessing Instructions

    Karl Storz ureteroscopes are being recalled because their instructions contain reprocessing procedures that have not been reviewed or approved by the FDA. The recall affects 3,069 units distributed nationwide.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide