The Recall Desk

State

South Carolina product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53851–53875 of 80980

  • ModerateFDA (Drugs)·D-0858-2016·2016-06-01

    Lymol Medical Recalls Sclerosol Intrapleural Aerosol Due to Defective Valve

    Lymol Medical is recalling Sclerosol Intrapleural Aerosol because a defective stem valve may cause the canister to leak propellant, resulting in no drug or an inadequate dose being delivered.

    Product
    Sclerosol Intrapleural Aerosol (sterile talc powder), Intrapleural administration, 4 g Canister, Rx Only, Distributed by: Bryan Corporation, Woburn, MA 01801, USA, NDC 63256-100-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0857-2016·2016-06-01

    Pfizer Recalls Zoloft Tablets Due to Thick Tablet Specifications

    Pfizer is recalling 68,214 bottles of Zoloft 100 mg tablets because some tablets were thicker than specifications. The recall covers nationwide distribution and Puerto Rico.

    Product
    Zoloft (sertraline HCl) tablets, 100 mg*, 30 count bottles, Rx only, Distributed by Roerig, Division of Pfizer, Inc., NY NY 10017, NDC 0049-4910-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1710-2016·2016-06-01

    Synthes 3.2 mm Radiolucent Drill Bits Recalled for Sterile Packaging Compromise

    Synthes (USA) Products LLC is recalling 1,274 sterile 3.2 mm radiolucent drill bits because the protective cap may not be secured, risking puncture of the sterile barrier.

    Product
    3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile Product Usage: The 3.2 mm Three-fluted Drill Bits are instruments that can be used with the following systems: Expert Lateral Femoral Nail (part number 03.010.060S only), Expert Tibial Nail, Expert Humeral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1790-2016·2016-06-01

    American Surgical Delicot Sponges Recalled for Packaging Sterility Defects

    American Surgical Company is recalling 338 boxes of Delicot sponges because defective packaging compromises sterility. The products were distributed worldwide.

    Product
    American Surgical Delicot 30 mm x 70 mm Ref Number: 63-10 Product Usage: Neurosurgical and Nonneurosurgical Sponges
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1813-2016·2016-06-01

    Volcano Cardiology Imaging Systems Recalled for Network Compatibility Reboot Issue

    Volcano Corporation is recalling specific cardiology imaging systems due to a software incompatibility that can cause unexpected reboots when encountering specific hospital network data.

    Product
    Volcano s5, s5i, CORE and CORE Mobile systems with software version 3.4 and v3.4 software kits. Cardiology: The Volcano Universal (Core /Core Mobile), S5iz Platform Imaging System is used for the qualitative and quantitative evaluation of vascular morphology in the coronary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1709-2016·2016-06-01

    Synthes 3.2 mm Drill Bits Recalled for Sterile Packaging Compromise

    Synthes (USA) Products LLC is recalling 7,363 sterile 3.2 mm three-fluted drill bits because the protective cap may not be secured, allowing the tip to puncture the sterile barrier.

    Product
    3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill Bits are instruments that can be used with the following systems: Expert Lateral Femoral Nail (part number 03.010.060S only), Expert Tibial Nail, Expert…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0875-2016·2016-06-01

    Akorn Recalls Chlorhexidine Gluconate Oral Rinse Due to Unknown Impurity

    Akorn, Inc. is recalling Chlorhexidine gluconate oral rinse due to an out-of-specification result for an unknown impurity.

    Product
    Chlorhexidine gluconate, oral rinse, 0.12% packaged in 16 fl. oz. (473 mL) PET bottle, Rx only, Manufactured by HI-TECH PHARMACAL CO., INC., Amityville, NY 11701, NDC 5083-0720-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·16V384000·2016-05-31

    Ford Recalls Vehicles Due to Air Bag Inflator Rupture Risk

    Ford is recalling specific 2005-2011 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    FORD — FORD, MERCURY, LINCOLN MUSTANG, MILAN, ZEPHYR, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V385000·2016-05-31

    Winnebago Recalls 2015-2016 Motor Homes for Steering Box Defect

    Winnebago is recalling 2015-2016 Tour and Itasca Ellipse motor homes because a steering box defect could cause loss of steering ability.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TOUR, ELLIPSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16182·2016-05-31

    Mirka Recalls Electric Random Orbital Sanders Due to Fire Hazard

    Mirka is recalling approximately 2,500 electric random orbital sanders sold in the U.S. because they can short circuit, posing a fire hazard.

    Product
    Random orbital sanders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V380000·2016-05-31

    Nissan Recalls 2013-2014 Pathfinder Vehicles for Brake Light Switch Defect

    Nissan is recalling 2013-2014 Pathfinder vehicles because an incorrectly installed brake light switch may cause brake lights to stay on or allow shifting out of Park without braking.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E049000·2016-05-27

    Xperion Recalls CNG Fuel Tanks Due to Leak Risk

    Xperion is recalling specific CNG fuel tanks because a neck adapter may pull out, allowing fuel to leak and increasing fire risk.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V373000·2016-05-27

    Jaguar Recalls 2009-2011 XF Models for Air Bag Inflator Rupture Risk

    Jaguar is recalling 2009-2011 XF vehicles in specific states because passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V376000·2016-05-27

    Audi Recalls 2008-2009 A4, A5, and Q5 for Air Bag Control Unit Defect

    Volkswagen Group of America is recalling 2008-2009 Audi A4, A5, and Q5 vehicles because the air bag control units may corrode and fail, potentially preventing air bag deployment in a crash.

    Product
    AUDI — AUDI A5, Q5, A4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V374000·2016-05-27

    Land Rover Recalls Range Rovers Due to Air Bag Inflator Rupture Risk

    Jaguar Land Rover is recalling 2007-2011 Range Rovers in specific US regions because passenger air bag inflators may rupture during deployment, potentially causing serious injury.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V375000·2016-05-27

    Coach and Equipment Recalls Buses with Defective Wheelchair Lifts

    Coach and Equipment is recalling 2014-2015 Metro Lite, Pegasus, and Phoenix buses because wheelchair lift platforms may crack or separate, posing an injury risk to operators.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, PEGASUS, METRO LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16179·2016-05-27

    Tommee Tippee Sippee Cups Recalled Due to Mold Risk in Valves

    Mayborn USA is recalling 3.1 million Tommee Tippee Sippee cups because mold can grow in the white valve, posing a risk of gastrointestinal symptoms.

    Product
    Tommee Tippee Sippee spill-proof cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16177·2016-05-26

    Rheem Recalls Electric Water Heaters Due to Fire and Burn Hazards

    Rheem is recalling about 54,000 Performance Platinum electric water heaters sold at Home Depot because the control panel can overheat, posing fire and burn risks.

    Product
    Rheem electric water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V366000·2016-05-26

    Daimler Trucks Recalls 2015-2016 FCCC Trucks for Steering Defect

    Daimler Trucks North America is recalling 2015-2016 FCCC trucks because a steering box defect could cause sudden loss of steering ability.

    Product
    FCCC — FCCC XBR, XCM, XCR, XBP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V370000·2016-05-26

    Ducati Recalls 2016 XDiavel S Motorcycles Due to Rear Wheel Installation Defect

    Ducati is recalling 925 model year 2016 XDiavel S motorcycles because the rear wheel may be incorrectly installed, which could cause a loss of braking and power transmission, increasing crash risk.

    Product
    DUCATI — DUCATI XDIAVEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V363000·2016-05-26

    Mercedes-Benz Recalls Vehicles Due to Air Bag Inflator Rupture Risk

    Mercedes-Benz is recalling specific 2008-2011 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C300, C350, C63, GLK350
    Category
    Vehicle
    Distribution
    Distributed nationwide