The Recall Desk

State

South Carolina product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44351–44375 of 80962

  • ModerateFDA (Drugs)·D-0243-2018·2018-02-07

    Neutrogena Acne Proofing Cleanser Recalled for Container Leakage

    Johnson & Johnson is recalling Neutrogena Acne Proofing whipped foam cleanser because the containers may leak propellant and product.

    Product
    Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, NET WT. 5 OZ (141 g) , Distributed by Johnson & Johnson Consumer Inc. Skillman, NJ 08558, UPC 0 70501 11131 4
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2018·2018-02-07

    Medline Newborn Kit Recalled for Subpotent Povidone-Iodine Prep Pads

    Medline Industries is recalling 288 cases of Newborn Kits because the Povidone-Iodine prep pads contain subpotent iodine, falling below the 0.85% label claim.

    Product
    Medline Newborn Kit. Packaged for Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0251-2018·2018-02-07

    Premier Pharmacy Labs Recalls Mitomycin Vials Due to Labeling Error

    Premier Pharmacy Labs is recalling 193 vials of Mitomycin 40 mg/mL due to a label error on the declared strength.

    Product
    Mitomycin 40 mg/mL Preservative Free Irrigation Volume: 10 mL SDV , Compounded by: Premier Pharmacy Labs 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-160-35.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0415-2018·2018-02-07

    Exactech Recalls 30 Equinoxe Shoulder Implants Due to Mislabeling

    Exactech is recalling 30 Equinoxe shoulder implants because they may be mislabeled. The devices were distributed to facilities in 15 US states, Puerto Rico, and Switzerland.

    Product
    Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the…
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0414-2018·2018-02-07

    Exactech Recalls 30 Mislabeled Equinoxe Shoulder Implant Components

    Exactech is recalling 30 Equinoxe Cage, Glenoid, Alpha, Small components due to potential mislabeling. The devices were distributed to facilities in 15 US states, Puerto Rico, and Switzerland.

    Product
    Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the…
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-0269-2018·2018-02-07

    Medline Sheath Removal Kit Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling 40 cases of Sheath Removal Kits because the iodine concentration is below the labeled claim.

    Product
    Medline Sheath Removal Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60063
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0682-2018·2018-02-07

    Jarrow Formulas Liquid L-Carnitine Recalled Due to Microbial Testing Results

    Jarrow Formulas is recalling one lot of Liquid L-Carnitine because a higher-than-normal micro result was found during testing.

    Product
    Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0296-2018·2018-02-07

    Medline Recalls Subpotent Povidone-Iodine Catheter Insertion Trays

    Medline Industries is recalling sterile catheter insertion trays because the iodine concentration in the prep pads is below the labeled claim.

    Product
    Liberator Medical Supply Catheter Insertion Tray, Sterile, Single Use Only. Distributed by: Liberator Medical Supply, INC. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0473-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, RH 130 DEG 13MM X 300MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0457-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 9MM X 360MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0450-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 11MM X 440MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0426-2018·2018-02-07

    Fresenius Kabi Recalls Vecuronium Bromide Vials Due to Impurity Failure

    Fresenius Kabi USA is recalling 35,620 vials of Vecuronium bromide for Injection due to an out-of-specification result for a related compound.

    Product
    Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India, NDC 63323-781-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0418-2018·2018-02-07

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets because stability testing showed out-of-specification results for total degradation impurities.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0420-2018·2018-02-07

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures

    Dr. Reddy's is recalling 12,579 bottles of Atorvastatin Calcium 40 mg tablets because they failed impurity specifications during stability testing.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0419-2018·2018-02-07

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 20 mg tablets because stability testing revealed out-of-specification total degradation impurities.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·009-2018·2018-02-06

    Guymon Extracts Recalls Fully Cooked Pork Products Due to Processing Deviation

    Guymon Extracts Inc. is recalling approximately 4,202 pounds of fully cooked pork products due to a processing deviation that may have allowed pathogen growth.

    Product
    Guymon Extracts, Inc — Guymon Extracts, Inc. Recalls Fully Cooked Pork Products Due to Possible Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18094·2018-02-06

    Lenovo Recalls ThinkPad X1 Carbon Laptops Due to Fire Hazard

    Lenovo is recalling approximately 78,000 ThinkPad X1 Carbon 5th Generation laptops in the US due to a potential fire hazard caused by an unfastened screw.

    Product
    ThinkPad X1 Carbon Laptops (5th Generation)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18721·2018-02-06

    Kohler Recalls Gasoline Engines Due to Fuel Leak and Fire Risk

    Kohler is recalling about 24,000 gasoline engines used in outdoor power equipment due to a faulty fuel cap that poses a fire hazard.

    Product
    Kohler gasoline engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V094000·2018-02-05

    Ferrara Recalls Fire Trucks Due to Corroding Pressure Valve Rings

    Ferrara is recalling specific fire-fighting vehicles because corroding rings may cause pressure relief valves to open, reducing water pressure and hindering fire-fighting efforts.

    Product
    INTERNATIONAL — INTERNATIONAL, KENWORTH, FERRARA 4400, T370, INFERNO, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V090000·2018-02-02

    Jaguar Recalls 2018 Models for Fuel Rail Leak Fire Risk

    Jaguar is recalling 2018 XE, XF, E-PACE, F-PACE, and F-TYPE vehicles because fuel rail end caps may leak, increasing the risk of a fire.

    Product
    JAGUAR — JAGUAR XF, E-PACE, F-TYPE, F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide