The Recall Desk

State

South Carolina product recalls

73,598 recalls have nationwide distribution and so reach South Carolina. 7,146 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,146
Critical
1,275
Severe
2,169
Most recent
2026-10-14

Of the 7,146 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.

Which agencies issued them

These figures cover only the 7,146 recalls whose distribution notice names South Carolina specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28951–28975 of 80744

  • LowFDA (Devices)·Z-0789-2021·2021-01-13

    Steris Recalls Vis-U-All High Temperature Tubing Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices inside the pouch.

    Product
    Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Model Number: 881091
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V005000·2021-01-12

    Smeal Recalls 2020 Aerial and Pumper Vehicles for Remote Controller Defect

    Smeal is recalling 2020 Aerial and Pumper vehicles because a wireless remote controller defect may cause batteries to discharge faster, potentially hindering firefighting efforts.

    Product
    SMEAL — SMEAL AERIAL, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E003000·2021-01-12

    Strategic Sports Recalls Simpson Shorty OTW Motorcycle Helmets

    Strategic Sports is recalling 3,752 Simpson Shorty OTW helmets that lack proper retention and protection, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V003000·2021-01-08

    Braun Recalls Crestline Ambulances Due to Defective Seat Belt Fasteners

    Braun Ambulances is recalling specific Crestline CCL150 ambulances because defective seat belt fasteners may fail, increasing injury risk in a crash.

    Product
    CRESTLINE COACH — CRESTLINE COACH CCL150 TYPE III, CCL150 TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V002000·2021-01-08

    Marion Body Works Recalls 2018 Freightliner M2 License Plate Light

    Marion Body Works is recalling one 2018 Freightliner M2-106 vehicle because a license plate light may be aimed at other drivers, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V001000·2021-01-07

    Volvo Recalls 2021 Models for SRS Control Unit Attachment Defect

    Volvo is recalling 2021 V60, V90, XC60, and XC90 models because the SRS control unit may detach during a crash, reducing occupant protection.

    Product
    VOLVO — VOLVO XC60, XC90, V60, V60CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21718·2021-01-07

    Noble House Recalls Chests and Cabinets Due to Tip-Over Hazards

    Noble House Home Furnishings is recalling four models of chests, cabinets, and dressers because they are unstable and can tip over, posing serious hazards to children.

    Product
    Chests, cabinets and dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21717·2021-01-07

    John Deere Recalls Frontier Rotary Tillers Due to Injury Hazard

    John Deere is recalling Frontier rotary tillers because some lack a safety sign warning of entanglement hazards. No injuries have been reported.

    Product
    Frontier model rotary tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0220-2021·2021-01-06

    WishGarden Herbs Recalls Goldenseal Powder Jars Due to Microbial Contamination

    WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.

    Product
    Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0218-2021·2021-01-06

    Wishgarden Herbs Recalls Happy Ducts Compress Due to Microbial Contamination

    Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.

    Product
    Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0177-2021·2021-01-06

    Imprimis Recalls Dexamethasone-Moxifloxacin Injection Due to Sterility Concerns

    Imprimis NJOF, LLC is recalling 6,520 vials of Dexamethasone-Moxifloxacin PF Injection because 13 vials were found with faulty crimps, raising concerns about sterility.

    Product
    Dexamethasone - Moxifloxacin PF Injection (1/5) mg/mL, Imprimis Rx Volume: 1mL/vial, Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ - 07852 (844)446-6979
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0747-2021·2021-01-06

    FDA Recalls Covidien TA Auto Suture Vascular Staplers Due to Damaged Components

    The FDA is recalling specific lots of Covidien TA Auto Suture Vascular Staplers because a damaged internal component may prevent adequate hemostasis or cause tissue damage.

    Product
    Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0766-2021·2021-01-06

    BD Phoenix PMIC-110 Recalled for False SXT Resistance Results

    Becton Dickinson & Co. is recalling BD Phoenix PMIC-110 IVDs due to false resistant SXT results with S. aureus, which could impact antibiotic treatment.

    Product
    BD Phoenix PMIC-110: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 449036:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21064·2021-01-06

    Massimo Percussion Massage Guns Recalled Due to Fire Hazard

    Massimo Motor Sports is recalling percussion massage guns sold at Costco because the lithium-ion battery can overheat and cause fires.

    Product
    Massage Guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0761-2021·2021-01-06

    BD Phoenix PMIC-107 Recalled for False SXT Resistance Results

    Becton Dickinson is recalling BD Phoenix PMIC-107 IVDs because false resistant results for S. aureus could lead to reduced treatment effectiveness.

    Product
    BD Phoenix PMIC-107: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448417
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0748-2021·2021-01-06

    FDA Recalls Covidien TA Auto Suture Vascular Loading Units

    FDA is recalling specific lots of Covidien TA Auto Suture Vascular Loading Units due to a damaged internal component that may prevent adequate hemostasis.

    Product
    Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0181-2021·2021-01-06

    Cipla Recalls Esomeprazole Magnesium Packets Due to Cross-Contamination

    Cipla is recalling 284,610 packets of Esomeprazole Magnesium delayed-release oral suspension because the excipient Crospovidone is contaminated with theophylline.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0182-2021·2021-01-06

    Cipla Recalls Esomeprazole Magnesium Suspension Due to Theophylline Contamination

    Cipla is recalling Esomeprazole Magnesium for Delayed-Release Oral Suspension 20mg due to cross-contamination with theophylline in the excipient Crospovidone.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0219-2021·2021-01-06

    Recall of Cord Care Powder Due to Cronobacter Sakazakii Contamination

    A non-sterile Cord Care Powder product was recalled because testing found Cronobacter Sakazakii contamination, posing a potential health risk without confirmed illness reports.

    Product
    Cord Care POWDER, 0.25 oz. (7 g) plastic jars, Wishgarden Herbs, Inc., Boulder, CO 80301. UPC 6-56490 24730 4
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0741-2021·2021-01-06

    Westmed Elongated Oxygen Mask Recalled for Loose Tube Connection

    Westmed is recalling 3,000 units of the REF 3102-E Elongated Oxygen Mask because the tube connection may become loose, potentially delaying oxygen therapy.

    Product
    REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2021·2021-01-06

    BD Phoenix PMIC-109 Recalled for False SXT Resistance Results

    Becton Dickinson is recalling BD Phoenix PMIC-109 in vitro diagnostic devices because they may produce false resistant results for S. aureus, potentially affecting antibiotic treatment choices.

    Product
    BD Phoenix" PMIC-109: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448419
    Category
    Medical Device
    Distribution
    Distributed nationwide