The Recall Desk

State

South Carolina product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42051–42075 of 80962

  • HighFDA (Devices)·Z-2237-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure

    Zimmer Biomet is recalling 832 trauma guide wires because packaging defects may compromise sterility, posing a risk of infection.

    Product
    G-PIN 2.8BL 3.2PL 98CM 2PK; 467260 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure

    Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.

    Product
    DRILL PT GUIDE WIRE 3.2MMX98CM, 469360 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2239-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Packaging Defects

    Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.

    Product
    BEAD TIP GD WIRE 3.0MM X 60CM; 29402 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2236-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure

    Zimmer Biomet is recalling 361 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.

    Product
    G-PIN 2.8BL 3.2PL 60CM 2PK; 467265 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2241-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure

    Zimmer Biomet is recalling 248 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.

    Product
    RECON DRILL 6MM X 439MM; 14-443023 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2240-2018·2018-06-27

    Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure

    Zimmer Biomet is recalling 304 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.

    Product
    3.2MM X 510MM COCR THD TIP; 14-443053 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0886-2018·2018-06-27

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium tablets because they failed impurities and degradation specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0888-2018·2018-06-27

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures

    Dr. Reddy's Laboratories is recalling 130,081 bottles of Atorvastatin Calcium 40 mg tablets nationwide due to failed impurity and degradation specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2270-2018·2018-06-27

    Olympus JF-160F Duodenoscopes Recalled for New Reprocessing Procedures

    Olympus Corporation of the Americas is recalling 68 JF-160F duodenoscopes nationwide to implement validated new reprocessing procedures.

    Product
    Olympus JF-160F duodenoscopes (Model NumberJF-160F)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0878-2018·2018-06-27

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Foreign Object

    Dr. Reddy's Laboratories is recalling 6,397 bottles of Atorvastatin Calcium 80 mg tablets because a foreign object was found embedded in a tablet.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2261-2018·2018-06-27

    Paragon 28 Recalls P28 JAWS Nitinol Staple Kits Due to Missing Drill Guide

    Paragon 28, Inc. is recalling P28 JAWS Nitinol Staple System kits because the drill guide is missing from the package.

    Product
    P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0887-2018·2018-06-27

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures

    Dr. Reddy's Laboratories is recalling specific lots of Atorvastatin Calcium tablets because they failed impurity and degradation specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V433000·2018-06-26

    KME Predator Emergency Vehicles Recalled for Lifting Device Defect

    KME is recalling 13 Predator emergency vehicles because tip-mounted lifting devices do not meet safety load ratings, posing an injury risk.

    Product
    KME — KME PREDATOR, PREDATOR SS AERIAL, PREDATOR SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V432000·2018-06-26

    Lexus Recalls Vehicles for Fuel Leak Fire Risk

    Toyota is recalling specific Lexus models because fuel pulsation dampers may crack and leak, increasing the risk of a fire.

    Product
    LEXUS — LEXUS GS 350, IS 350, IS 350C, GS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18181·2018-06-26

    Huish Outdoors Recalls Scuba Diving Regulators Due to Drowning Hazard

    Huish Outdoors is recalling Oceanic and Hollis scuba diving regulators because they can restrict airflow at low tank pressures, posing a drowning hazard to divers.

    Product
    Oceanic and Hollis scuba diving regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V430000·2018-06-25

    Audi Recalls 2013-2015 S8 and A8 Models for Fuel Leak Risk

    Volkswagen Group of America is recalling 2013-2015 Audi S8 and A8 vehicles because a fuel supply line may leak, increasing fire risk.

    Product
    AUDI — AUDI A8, S8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V429000·2018-06-25

    Keystone Recalls 2019 Summerland Trailers Due to Incorrect Tire Label

    Keystone is recalling 2019 Summerland recreational trailers because the Federal Identification Label lists an incorrect tire rim size, which could lead to improper rim replacement.

    Product
    KEYSTONE — KEYSTONE SUMMERLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V424000·2018-06-25

    Spartan Emergency Vehicles Recalled for Fire Pump Solenoid Corrosion

    Spartan Motors is recalling 2009-2018 Gladiator and MetroStar emergency vehicles because internal corrosion in the fire water pump solenoid may cause loss of water pressure, increasing injury risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V427000·2018-06-22

    Audi Recalls A4, A6, and RS4 Models Due to Air Bag Inflator Defect

    Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    AUDI — AUDI A4, A6, RS 4, RS4
    Category
    Vehicle
    Distribution
    Distributed nationwide