The Recall Desk

State

South Carolina product recalls

72,969 recalls have nationwide distribution and so reach South Carolina. 7,117 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,117
Critical
1,268
Severe
1,870
Most recent
2026-09-16

Of the 7,117 recalls naming South Carolina we have scored against our rubric, 1,268 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (26%) are Severe.

These figures cover only the 7,117 recalls whose distribution notice names South Carolina specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6076–6100 of 80086

  • HighCPSC·25408·2025-07-24

    Pura 4 diffuser cover magnets can detach, posing an ingestion hazard

    The detachable cover of the Pura 4 Smart Home Fragrance Diffuser is being recalled because its magnets can detach. Three reports of magnets detaching have been received. About 851,400 units affected.

    Product
    Pura 4 Smart Home Fragrance Diffusers with detachable covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25397·2025-07-24

    Georgia Pine turpentine bottles lack the required child-resistant packaging

    Georgia Pine Gum Spirits of Turpentine in 4 oz glass bottles is being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 20,000 units affected.

    Product
    Georgia Pine Gum Spirits of Turpentine Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25399·2025-07-24

    Creekwood Naturals turpentine bottles lack the required child-resistant packaging

    Creekwood Naturals Gum Spirits of Turpentine bottles are being recalled because they violate the mandatory standard for child-resistant packaging. About 9,000 units are affected.

    Product
    100% Natural Pure Gum Spirits of Turpentine Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25401·2025-07-24

    LIVACTI retractable safety gates leave a gap a child can pass

    LIVACTI retractable mesh safety gates, model LT-BG01-3, are being recalled because a child's torso can fit through the opening between the gate and the floor. About 1,400 units are affected.

    Product
    LIVACTI Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25404·2025-07-24

    Minecraft light-up slap bracelets allow children to access button cell batteries

    Minecraft Light-Up Slap Ruler Bracelets are being recalled because the battery compartment can be opened easily by children, violating the mandatory toy standard. About 75,900 units affected.

    Product
    Minecraft Light-Up Slap Ruler Bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V483000·2025-07-24

    2026 Cadillac VISTIQ High-Voltage Battery Bolt Defect Recall

    General Motors is recalling certain 2026 Cadillac VISTIQ and 2025 Cadillac LYRIQ vehicles because bolts attaching the high-voltage battery to the floor may be missing or loose, creating a fire risk in a crash.

    Product
    CADILLAC — CADILLAC VISTIQ, LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V481000·2025-07-23

    Tiffin motorhome alternator programming error can stall the engine

    Tiffin is recalling certain 2023-2026 motorhomes with 2.0 litre engines because the secondary alternator controller programming was not properly updated, which can stall the engine.

    Product
    TIFFIN — TIFFIN GH1, GT1, CONVOY, GH2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V479000·2025-07-23

    Ferrari Purosangue fuse box contact can decrease braking ability

    Ferrari is recalling certain 2023-2025 Purosangue vehicles because the fuse box power supply and passenger-side footrest may contact each other, causing a short circuit that decreases braking ability.

    Product
    FERRARI — FERRARI PUROSANGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V395000·2025-07-23

    BMW electric drive motor software can shut down high voltage system

    BMW is recalling certain 2022-2025 i4, 2022-2024 iX, 2023-2024 i7 and 2024 i5 vehicles because electric drive motor software may shut down the high-voltage system, causing a loss of drive power.

    Product
    BMW — BMW I5, IX, I7, I4 EDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0305-2025·2025-07-23

    Dubai emek pistachio cacao spread may be contaminated with Salmonella

    Dubai emek Spread Pistachio Cacao Cream with Kadayif is being recalled after the FDA notified the firm that the product may be contaminated with Salmonella. 316 cases are affected.

    Product
    Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik Urunlerilkl. Gida Turkey
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2102-2025·2025-07-23

    i-view video laryngoscopes may be faulty because of depleted batteries

    The i-view video laryngoscope is being recalled because of the potential for faulty devices as a result of depleted batteries. 2,152 pieces are affected.

    Product
    i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·H-0287-2025·2025-07-23

    Crumbled cookie bars recalled over potential Listeria monocytogenes contamination

    Crumbled Cookie Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Crumbled Cookie Bar (85200), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0285-2025·2025-07-23

    Strawberry Shortcake bars recalled over potential Listeria monocytogenes contamination

    Strawberry Shortcake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Strawberry Shortcake Bar (85050), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0304-2025·2025-07-23

    YoCrunch strawberry and raspberry granola yogurt may contain plastic pieces

    A YoCrunch Lowfat Yogurt with Toppers two-product package containing strawberry and raspberry yogurt with granola is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers Two-product package. Contains 8-6oz (170g) cups of Strawberry Yogurt with Granola pieces (Cup UPC 46675-00010), and 8-6oz (170g) cups of Raspberry Yogurt with Granola pieces (Cup UPC 46675-01401). Two- Pack, UPC 46675-01401. Keep Refrige
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0300-2025·2025-07-23

    YoCrunch strawberry yogurt with M&M toppers may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis candies, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00083 2. Multipack containing 4-4 oz. cups UPC 46675-01312 Keep Refrigerated. Distributed by Dano
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0303-2025·2025-07-23

    YoCrunch Snickers and Twix yogurt packages may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with Snickers and Twix pieces are being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bar pieces (cup UPC 46675-00113). Two-Pack UPC 46675-02614. Keep Refrigerat
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2025·2025-07-23

    NIO+ intraosseous device stabilizer may not release properly after insertion

    The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.

    Product
    Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2025·2025-07-23

    VITROS Performance Verifier II lots can cause quality control drift

    VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.

    Product
    Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/Catalog Number: 8231474 Software Version: N/A Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2025·2025-07-23

    VITROS CHE slides sold in Japan can cause quality control drift

    VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.

    Product
    VITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V482000·2025-07-23

    Hyundai IONIQ 5 battery bus bar may be improperly tightened

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0533-2025·2025-07-23

    Rizatriptan 5 mg tablets exceed the acceptable intake limit for nitrosamine

    Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2025·2025-07-23

    NIO-A intraosseous device stabilizer may not release properly after insertion

    The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.

    Product
    Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
    Category
    Medical Device
    Distribution
    Distributed nationwide