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.

48551–48575 of 80970

  • ModerateFDA (Devices)·Z-1749-2017·2017-04-12

    Siemens ADVIA Centaur BR Assay Recalled for Potential Syphilis Assay Interference

    Siemens is recalling ADVIA Centaur BR assays due to potential interference from the Syphilis assay, which may affect test accuracy.

    Product
    Siemens ADVIA Centaur BR assay Cat No. 09010686, SMN 10340081 (5-pack/250 tests - REF) BR Assay for CA 27.29 The ADVIA Centaur¿ BR assay is an in vitro diagnostic test for the quantitative serial determination of cancer antigen CA 27.29 in human serum using the ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1712-2017·2017-04-12

    Siemens ADVIA Chemistry Enzyme 2 Calibrator Recalled for Positive Bias

    Siemens is recalling ADVIA Chemistry Enzyme 2 Calibrators due to a positive bias of up to 41% in AST and AST_c assay results.

    Product
    ADVIA Chemistry Enzyme 2 Calibrator, multi-analyte mixture Product Usage: Assays included in Enzyme 2 Calibrator: AST, AST_c ALT, ALT_c, ALTP5P, ALTP_c, ASTP5P and ASTP_c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1727-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Card Issues

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Swedish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1720-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Norwegian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0630-2017·2017-04-12

    Alvogen Recalls Nifedipine Extended-Release Tablets Due to Cross-Contamination

    Alvogen, Inc. is recalling Nifedipine Extended-Release Tablets, 60 mg, due to cross-contamination with sorafenib powder found in the manufacturing facility's inlet air duct.

    Product
    Nifedipine Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-369-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0636-2017·2017-04-12

    G & W Laboratories Recalls Ciclopirox Olamine Cream Due to Outdated Insert

    G & W Laboratories is recalling 230,700 tubes of Ciclopirox Olamine Cream because some lots were packaged with an out-of-date package insert.

    Product
    CICLOPIROX OLAMINE — CICLOPIROX OLAMINE (CICLOPIROX OLAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1725-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Korean SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0649-2017·2017-04-12

    Dr. Reddy's Recalls Rivastigmine Tartrate Capsules Due to Cross-Contamination

    Dr. Reddy's is recalling Rivastigmine Tartrate Capsules because testing detected a peak for Ranitidine, indicating cross-contamination with other products.

    Product
    RIVASTIGMINE TARTRATE — RIVASTIGMINE TARTRATE (RIVASTIGMINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0633-2017·2017-04-12

    Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination

    Alvogen is recalling specific lots of Adalat CC (nifedipine) extended-release tablets due to cross-contamination with sorafenib powder.

    Product
    Adalat CC (nifedipine) Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749401
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V243000·2017-04-11

    Mercedes-Benz Recalls 2016-2017 C300 Vehicles for Steering Defect

    Mercedes-Benz is recalling 2016-2017 C300 vehicles because power steering motor contacts may be improperly welded, risking loss of steering assist and increased crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V251000·2017-04-11

    Mercedes-Benz Recalls 2017 Models for Front Seat Belt Pretensioner Defect

    Mercedes-Benz is recalling 12,743 2017 vehicles because front seat belt pretensioners may not function properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S550, S550 4MATIC, C 300, GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V247000·2017-04-11

    Mercedes-Benz Recalls 2013 R320 Due to Post-Crash Fire Risk

    Mercedes-Benz is recalling one 2013 R320 4MATIC CDI vehicle because the engine may not shut off after a crash, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ R320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V249000·2017-04-11

    Foretravel Recalls 2012-2018 Motorhomes Due to Front Suspension Defect

    Foretravel is recalling 2012-2018 Phenix, IH45, and Nimbus motorhomes because front suspension ball joints can loosen, potentially causing a loss of steering control.

    Product
    FORETRAVEL — FORETRAVEL NIMBUS, IH45, PHENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V250000·2017-04-11

    Mercedes-Benz Recalls G-Class Vehicles for Steering Coupling Wear

    Mercedes-Benz is recalling 2013-2016 G550, G63, and G65 vehicles because an insufficiently tightened steering coupling may wear, potentially causing a loss of steering and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G63, AMG G65, G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V241000·2017-04-11

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Water Ingress

    Mercedes-Benz is recalling specific 2016-2017 models because an insufficiently sealed electric power steering connector may allow water to enter the control unit, potentially deactivating steering assist.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GL350, GLE63S, GLE300D, GLE350D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17739·2017-04-11

    John Deere Recalls Gator Utility Vehicles Due to Crash Hazard

    John Deere is recalling about 8,500 Gator Utility Vehicles because a loose dust boot on the throttle cable can prevent the vehicle from stopping, posing a crash hazard.

    Product
    Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V246000·2017-04-11

    Mercedes-Benz Recalls 2016-2017 E300 Vehicles for Spoiler Defect

    Mercedes-Benz is recalling 2016-2017 E300 and E300 4MATIC vehicles because the roof-mounted spoiler may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17129·2017-04-11

    Anaheim and Moen Recall Garbage Disposals Due to Impact Hazard

    Anaheim Manufacturing and Moen are recalling about 146,000 garbage disposals because a metal component can break off and exit the unit, posing an impact hazard.

    Product
    Garbage disposals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17128·2017-04-11

    Teavana Recalls Flip Tumblers Due to Hot Liquid Burn Hazard

    Starbucks is recalling Teavana Flip Tumblers because they can leak hot liquid, posing a burn risk. Consumers should stop using them and contact Starbucks for a refund.

    Product
    Teavana Flip Tumblers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V248000·2017-04-10

    Proline Cargo Trailer Recall for Short Wheel Nuts

    PROLine is recalling 2016-2017 Cargo trailers because short wheel nuts may allow wheels to detach, increasing crash risk.

    Product
    PROLINE — PROLINE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V239000·2017-04-10

    Thor Motor Coach Recalls 2017 Motorhomes Due to Incorrect Hitch Weight Labels

    Thor Motor Coach is recalling 2017 Ace, Hurricane, and Windsport motorhomes because tow hitch labels incorrectly state a 10,000 lb capacity instead of the actual 8,000 lbs.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR WINDSPORT, HURRICANE, ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide