The Recall Desk

State

South Carolina product recalls

73,741 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.

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38651–38675 of 80893

  • SevereNHTSA·19V143000·2019-02-28

    Chrysler Recalls 2018 Pacifica Models Due to Control Arm Separation Risk

    Chrysler is recalling 47,771 2018 Pacifica and Pacifica Plug-In Hybrid vehicles because the right front lower control arm may separate, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V141000·2019-02-28

    McLaren Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    McLaren is recalling specific 2012-2017 models because passenger air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    MCLAREN — MCLAREN MP4-12C SPIDER, 675 LONGTAIL, P1, 570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V149000·2019-02-28

    Subaru Recalls Vehicles for Brake Light Switch Malfunction Risk

    Subaru is recalling specific Impreza, WRX, Forester, and Crosstrek models because a faulty brake light switch may prevent lights from working or the vehicle from starting.

    Product
    SUBARU — SUBARU IMPREZA, WRX, FORESTER, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19076·2019-02-28

    Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging

    Clinical Resolution Laboratory is recalling Numb 100 Topical Anesthetic Cream because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk.

    Product
    Numb 100 Topical Anesthetic Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V147000·2019-02-28

    Triple E Recalls 2019 Serenity Motorhomes Due to Electrical Wiring Error

    Triple E is recalling 2019 Serenity S24CB motorhomes because a wiring error may prevent 120V outlets from being properly ground-fault protected, increasing the risk of electrical injury.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V145000·2019-02-28

    Diamond Coach Recalls 2018 Transit Buses Due to Seat Lock Failure

    Diamond Coach is recalling 2018 Transit MPV/VTUM and PT 2000 buses because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    DIAMOND COACH — DIAMOND COACH, DIAMOND COACH TRANSIT PT 2000, MPV/VTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V144000·2019-02-28

    Four Guys Recalls 2017-2018 Fire Apparatus Due to Brake Light Defect

    Four Guys is recalling 2017-2018 fire apparatus equipped with specific Whelen brake lights that may illuminate without the brake pedal being pressed.

    Product
    4 GUYS — 4 GUYS COMMERCIAL TANKER, COMMERCIAL PUMPER, CUSTOM RESCUE, CUSTOM PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0857-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling 57 PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70 w/trolley Government Bundle, Product 860352, Software revisions up to and including A.07.05. 22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0960-2019·2019-02-27

    Sysco Recalls Block and Barrel Cheddar Cheese Due to Temperature Issues

    Sysco Charlotte is recalling Block and Barrel Imperial Cheddar cheese because a cooler malfunction may have compromised food safety.

    Product
    Block and Barrel Imperial CHEESE CHEDDAR X SHARP LOAF YW 2/5 LB cases
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0508-2019·2019-02-27

    US Compounding Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 1,686 syringes of Ephedrine Sulfate 50 mg/10 mL because the company cannot ensure the product is sterile.

    Product
    Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR 800-718-3588, Barcode: 62295308407
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0850-2019·2019-02-27

    Baxter Recalls Kaguya Automated Peritoneal Dialysis Systems Due to Software Defect

    Baxter Healthcare is recalling 1,085 Kaguya Automated Peritoneal Dialysis Systems because a software defect may cause shortened dwell times during therapy.

    Product
    Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1001-2019·2019-02-27

    Sysco Recalls Majestic Blue Crab Meat Due to Temperature Control Failure

    Sysco Charlotte is recalling Majestic Blue Crab Meat Super Lump because a cooler malfunction meant the product was not held at appropriate temperatures, potentially making it unsafe.

    Product
    Majestic Blue CRAB MEAT SUPER LUMP PAST MEX
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0854-2019·2019-02-27

    Philips PageWriter TC50 ECG Devices Recalled for Overheating and Fire Risk

    Philips is recalling PageWriter TC50 electrocardiogram devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V135000·2019-02-27

    BMW Recalls 2019 X7 Models Due to Loose Seat Adapter Bolts

    BMW is recalling 2019 X7 vehicles with the business lounge seat option because seat adapter bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0501-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, USP, 100 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above the interim acceptable daily intake level.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 30-count (NDC: 13668-115-30), b) 90-count (NDC: 13668-115-90), c) 1000-count (NDC: 13668-115-10) per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0503-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0859-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30 w/ trolley Government Bundle, Product 860354, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0856-2019·2019-02-27

    Philips PageWriter TC20 Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC20 devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury.

    Product
    PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide