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.

45751–45775 of 80970

  • CriticalFDA (Drugs)·D-1087-2017·2017-08-23

    Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients

    Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.

    Product
    Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3367-2017·2017-08-23

    NatureAll Acidophilus-Plus Recalled for Undeclared Milk Allergens

    NatureAll is recalling Acidophilus-Plus dietary supplements because they contain undeclared milk allergens, including colostrum, dried yogurt, and whey.

    Product
    Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3038-2017·2017-08-23

    Boston Scientific Recalls Emblem MRI S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2017·2017-08-23

    Hardcore Formulations Recalls D-ZINE Rapid Size and Strength Capsules

    Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.

    Product
    D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3034-2017·2017-08-23

    Cenorin ThermaSure Medical Device Dryers Recalled for Overheating Terminal Block

    Cenorin, LLC is recalling 18 ThermaSure Series 1000 medical device dryers because a manufacturing defect causes the terminal block to overheat, char, or burn.

    Product
    ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1084-2017·2017-08-23

    FDA Recalls Ultra-Sten Capsules Marketed Without Approval

    Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.

    Product
    ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1091-2017·2017-08-23

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.

    Product
    0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3039-2017·2017-08-23

    Boston Scientific Recalls SQ-RX 1010 Pulse Generators Due to Memory Corruption

    Boston Scientific is recalling approximately 12,450 SQ-RX 1010 Pulse Generators because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    SQ-RX 1010 Pulse Generator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant ventricular tachycardia, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3037-2017·2017-08-23

    Boston Scientific Recalls Emblem S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 16,750 Emblem S-ICD devices because they may deliver atypical energy levels due to internal memory corruption.

    Product
    EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1093-2017·2017-08-23

    Lupin Recalls Mibelas 24 Fe Contraceptive Tablets Due to Sequence Error

    Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.

    Product
    Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17209·2017-08-23

    Nutrilife Recalls 29% Hydrogen Peroxide Bottles Due to Fire and Burn Hazards

    Nutrilife is recalling 29% hydrogen peroxide bottles because caps may not vent properly, allowing pressure to build and cause rupture, posing fire and burn risks.

    Product
    Nutrilife 29% hydrogen peroxide (H202) one-gallon bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3368-2017·2017-08-23

    FDA Recalls Metabo-Plus Dietary Supplement for Undeclared Milk Allergen

    NatureAll-STF Holding, LLC is recalling 254 bottles of Metabo-Plus dietary supplement because it contains undeclared milk (whey), a major allergen.

    Product
    Metabo-Plus, Garlic/Papaya Plus, No. 103, 90 Capsules, Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3366-2017·2017-08-23

    Aldi Gluten Free Hamburger Buns Recalled for Undeclared Eggs

    Silver Hills Bakery is recalling Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns due to undeclared eggs. The recall affects 9,639 retail units sold nationwide.

    Product
    Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns, 11.3 Ounces, in plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3369-2017·2017-08-23

    NatureAll Thymus Plus Recalled for Undeclared Milk Allergen

    NatureAll is recalling Thymus Plus dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.

    Product
    Thymus Plus, No. 114, 90 Capsules, Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2720-2017·2017-08-23

    High Liner Breaded Fish Recalled for Undeclared Milk Allergen

    High Liner Foods is recalling Oven Ready Whole Grain Breaded Fish Sea Wonders due to potential undeclared milk. Consumers with milk allergies should not consume the product.

    Product
    HFS 1/10 Oven Ready Whole Grain Breaded Fish Sea Wonders, Item Number: 26533
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2800-2017·2017-08-23

    High Liner Salmon Recalled for Undeclared Milk Allergen

    High Liner Foods is recalling Uppercrust Honey Chipotle Salmon nationwide due to undeclared milk, a major food allergen.

    Product
    HLSC 10LB Uppercrust Honey Chipotle Salmon 5.71oz., Item Number: A1222
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2675-2017·2017-08-23

    High Liner Recalls Beer Battered Fish Fillets Due to Undeclared Milk

    High Liner Foods Inc. is recalling Best Choice Beer Battered Fish Fillets because the product may contain undeclared milk.

    Product
    Best Choice 12/18.2oz Beer Battered Fish Fillets, Item Number: SB1401
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2762-2017·2017-08-23

    High Liner Alaska Pollock Sticks Recalled for Undeclared Milk

    High Liner Foods is recalling HFS 4/5 Oven Ready Whole Grain Breaded Alaska Pollock Sticks because the product may contain undeclared milk.

    Product
    HFS 4/5 Oven Ready Whole Grain Breaded Alaska Pollock Sticks. Item Number: 1089867
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2781-2017·2017-08-23

    High Liner Foods Recalls Breaded Alaska Pollock Nuggets for Undeclared Milk

    High Liner Foods is recalling Gordon Food Service breaded Alaska pollock nuggets because they may contain undeclared milk.

    Product
    Gordon Food Service 2/5LB Whole Grain Breaded Alaska Pollock Nugget 1oz ., Item Number: 10026693
    Category
    Food
    Distribution
    Distributed nationwide