The Recall Desk

State

South Carolina product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57701–57725 of 80986

  • ModerateFDA (Devices)·Z-2783-2015·2015-09-23

    Siemens ACUSON SC2000 Ultrasound System Recalled for Data Capture Error

    Siemens is recalling ACUSON SC2000 ultrasound systems because a software error prevents the capture of images or clips when patient names are registered with different capitalization.

    Product
    ACUSON SC2000 Ultrasound System with software versions VB10B and lower; Model 10433816; Product Usage: The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2765-2015·2015-09-23

    Boston Scientific WATCHMAN Device Field Correction for Hemostasis Valve Cross-Thread Risk

    Boston Scientific is issuing a field correction for WATCHMAN Left Atrial Appendage Closure Devices to prevent hemostasis valve cross-threading and potential blood leakage.

    Product
    Boston Scientific, WATCHMAN Left Atrial Appendage Closure Device with Delivery System, 21mm x 12F ( M635WU21060, WU21060, 24mm x 12F(M635WU24060, WU2406) , 27mm x 12F(M635WU27060, WU2706) , 30mm x 12F(M635WU30060, WU3006) , 33mm x 12F( M635WU33060, WU3306). For cardiac use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2763-2015·2015-09-23

    Med Tec Recalls CIVCO Shoulder Retractors Due to Excessive Strap Length

    Med Tec Inc is recalling CIVCO Shoulder Retractors because the wrist straps used for patient positioning are too long.

    Product
    CIVCO Shoulder Retractors, Reusable non-sterile hand grip, REF 302070, packaged 1 set per box, RX. For use in patient positioning. The grips are used for pulling down the shoulders during radiotherapy simulation and treatment sessions where opposed lateral fields are used in…
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0418-2015·2015-09-23

    Hospira Recalls Ketamine Hydrochloride Injection Due to Cracked Vials

    Hospira is recalling 83,320 vials of Ketamine Hydrochloride Injection because customer complaints reported cracked and leaking glass vials.

    Product
    Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2768-2015·2015-09-23

    MedTest DX Control Reconstitution Fluid Recalled for Fill Volume Variation

    MedtestDx, Inc. is recalling 79 kits of MedTest DX Control Reconstitution Fluid due to vial fill volume variations that may cause control results to fall outside suggested ranges.

    Product
    MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 ml. Bottle: 5 ml amber glass Cap: 18 mm white seal plug seal rubber HC-DIL (Human Control Diluent) is reagent grade water filled into 5ml vials used to reconstitute Human controls HNC200 and HEC200. in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1814-2015·2015-09-23

    Apotex Recalls Cevimeline Hydrochloride Capsules Due to Stability Failures

    Apotex Inc. is recalling Cevimeline Hydrochloride Capsules, 30 mg, because the product may not meet specification limits for assay testing.

    Product
    Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b) 500 count bottle, Rx Only, Manufactured by: Apotex Research Pvt., Ltd., Bangalore, India, Manufactured for: Apotex Corp, Westin, FL, a) NDC 60505-3145-1, b) NDC 60505-3145-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1813-2015·2015-09-23

    EMD Serono Recalls Clomiphene Citrate Tablets Due to Chemical Contamination

    EMD Serono is recalling specific lots of Clomiphene Citrate tablets because the active ingredient failed due to chemical contamination.

    Product
    ClomiPHENE CITRATE Tablets, USP, 50 mg, 10-count (2 foil sealed plastic trays of 5 tablets each) per carton, Rx only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD., Jerusalem, 91010, Israel; Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2785-2015·2015-09-23

    RayStation Radiation Therapy Software Recalled for Display Errors

    RaySearch Laboratories is recalling RayStation software due to a floating-point precision error that affects the display of isodose lines and color tables.

    Product
    Radiation Therapy Treatment Planning System software RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2776-2015·2015-09-23

    Edwards Pressure Monitoring Kit Recalled for Flow Restriction Issues

    Edwards Lifesciences is recalling pressure monitoring kits due to flow restriction in the IV set, which may prevent system priming or line flushing.

    Product
    Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer. A sterile, single-use kit that monitors pressures when attached to pressure monitoring catheters. For use on patients requiring intravascular, intracranial, or intrauterine pressure monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1429-2015·2015-09-23

    Akorn Recalls IC-Green Injection Kits Due to Low Potency

    Akorn, Inc. is recalling 370 kits of IC-Green (indocyanine green for injection) because a low out-of-specification potency result was found.

    Product
    IC-GREEN (indocyanine green for injection, USP), 25 mg Kit (NDC 17478-701-02, UPC 3 17478-701-02 6) containing 6-count IC-Green Vials 25 mg (NDC 17478-701-25, barcode (01)00317478701255) and 6-count 10 mL Sterile Aqueous Solvent Ampules (NDC 17478-701-10, UPC 3 17478-701-10 1)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2773-2015·2015-09-23

    Pointe Scientific Creatinine Reagent Recall Due to Labeling Error

    Pointe Scientific is recalling 93 kits of Creatinine Reagent C7539-150 because the R1 and R2 reagent bottles are mislabeled, which prevents valid test results.

    Product
    Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro diagnostic C7539-150 kit includes one R1 and one R2 bottle. R1: HDPE plastic bottle. 120 ml fill. R2: HDPE plastic bottle. 90 ml fill.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V586000·2015-09-22

    Freightliner Trucks Recalled for Rear Brake Caliper Positioning Defect

    Daimler Trucks North America is recalling 2014-2016 Freightliner trucks because rear brake calipers may contact the spring suspension, reducing braking performance.

    Product
    FREIGHTLINER — FREIGHTLINER 114SD, BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V583000·2015-09-22

    KYMCO Recalls 2015 Super 8 Scooters Due to Brake Hose Routing Defect

    KYMCO is recalling 2015 Super 8-50 X and Super 8-150 X scooters because the front brake hose may contact the tire, risking brake failure and crashes.

    Product
    KYMCO — KYMCO SUPER 8-150 X, SUPER 8-50 X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V582000·2015-09-22

    Crossroads Sunset Trail Trailers Recalled for Kitchen Range Fire Risk

    Crossroads is recalling 2015-2016 Sunset Trail trailers because kitchen ranges lack an isolation panel, creating a risk of fire, explosion, or carbon monoxide buildup.

    Product
    CROSSROADS — CROSSROADS SUNSET TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V587000·2015-09-22

    Suzuki Recalls SX4 Vehicles for Power Steering Pump Seizure Risk

    Suzuki is recalling 2012-2013 SX4 vehicles because the power steering pump may seize, causing loss of steering assist and increasing crash risk.

    Product
    SUZUKI — SUZUKI SX4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V585000·2015-09-22

    Newmar Recalls Motorhomes Due to Exhaust Tube Fire Risk

    Newmar is recalling specific Dutch Star, Dutch Aire, and King Aire motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase fire risk.

    Product
    NEWMAR — NEWMAR DUTCH AIRE DP, DUTCH STAR, KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·15T020000·2015-09-22

    Michelin Recalls X Works Tires for Missing Required Markings

    Michelin is recalling specific X Works XZY tires because they lack required DOT symbols and load range letters, which may cause confusion with non-compliant tires.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E076000·2015-09-21

    Henderson Wheel Recalls Torsion Arm Assemblies Due to Detachment Risk

    Henderson Wheel is recalling torsion arm assemblies where the arm is too small for its housing, posing a risk of trailer detachment and loss of control.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V580000·2015-09-21

    MCI Recalls 2015 Motor Coaches Due to Fire Risk in Fuse Block

    Motor Coach Industries is recalling 145 model year 2015 D4000, D4005, D4500, and D4505 vehicles because an incorrectly assembled fuse block may cause arcing and increase the risk of a fire.

    Product
    MCI — MCI D4500, D4005, D4505, D4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V581000·2015-09-21

    Winnebago Recalls 2015-2016 Motorhomes Due to Wiring Fire Risk

    Winnebago is recalling 172 model year 2015-2016 Itasca Sunova and Winnebago Sightseer motorhomes because a wiring harness may be damaged, increasing the risk of fire.

    Product
    ITASCA — ITASCA, ITASCO, WINNEBAGO SUNOVA, SIGHTSEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·15V579000·2015-09-21

    Mitsubishi Recalls 2011 Outlander Sport for Incorrect Certification Labels

    Mitsubishi is recalling 2011 Outlander Sport vehicles manufactured on December 3, 2010, due to incorrect certification labels lacking the correct VIN. Dealers will install corrected labels free of charge.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V577000·2015-09-18

    Toyota Recalls RAV4 and RAV4 EV for Wiper Linkage Separation Risk

    Toyota is recalling 2009-2012 RAV4 and 2012-2014 RAV4 EV vehicles because water dripping on the wiper joint may cause corrosion and linkage separation, reducing visibility.

    Product
    TOYOTA — TOYOTA RAV4 EV, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·15245·2015-09-17

    Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Hazards

    Bed Handles Inc. is recalling about 113,000 portable bed handles that lack safety retention straps. The missing straps allow the handles to shift, creating gaps that pose a risk of entrapment, strangulation, and death.

    Product
    Portable bed handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide