The Recall Desk

State

South Carolina product recalls

73,737 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,152
Critical
1,275
Severe
2,169
Most recent
2026-10-28

Of the 7,152 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.

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32676–32700 of 80889

  • HighNHTSA·20V134000·2020-03-06

    Triple E RV Recalls 2020 Wonder Travel Trailers Due to Fire Risk

    Triple E Recreational Vehicles is recalling 2020 Wonder travel trailers because unprotected ceiling light wires can chafe and arc, increasing the risk of a fire.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E011000·2020-03-06

    Joyson Recalls Rear Seat Belt Retractors for Restraint Failure

    Joyson is recalling certain rear seat belt retractors because the locking mechanism may not properly restrain occupants, increasing injury risk in a crash.

    Product
    SEAT BELTS:REAR/OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20720·2020-03-05

    RH Recalls Camino Floor Lamps Due to Fire Hazard

    RH is recalling about 800 Camino floor lamps sold in the U.S. because the foot switch can overheat or catch fire, posing a fire hazard.

    Product
    Camino Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20086·2020-03-05

    ECHO and Shindaiwa Recall Backpack Blowers Due to Laceration Hazards

    ECHO and Shindaiwa are recalling about 67,700 backpack blowers and 6,600 replacement straps because parts can be expelled, posing laceration and impact risks.

    Product
    ECHO and Shindaiwa Backpack Blowers and replacement straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0863-2020·2020-03-04

    Taro Recalls Phenytoin Oral Suspension Due to Resuspension Issues

    Taro Pharmaceuticals is recalling two lots of Phenytoin Oral Suspension because the medication may coagulate and fail to resuspend as directed.

    Product
    PHENYTOIN — PHENYTOIN (PHENYTOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V131000·2020-03-04

    AEV Traumahawk Ambulances Recalled for Electrical Fire Risk

    Halcore Group is recalling 2018 AEV Traumahawk ambulances because an undersized power cord may cause an electrical short circuit, increasing the risk of fire or shock.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V132000·2020-03-04

    Peterbilt 320 and 520 Trucks Recalled for Brake Signal Hose Defect

    PACCAR is recalling 2016-2020 Peterbilt 320 and 520 trucks because a missing quick release valve may delay brake release, increasing crash risk.

    Product
    PETERBILT — PETERBILT 320, 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V130000·2020-03-04

    Peterbilt Trucks Recalled for Battery Cable Fire Risk

    PACCAR is recalling 2015-2020 Peterbilt trucks because a battery cable may chafe and cause an electrical short circuit, increasing fire risk.

    Product
    PETERBILT — PETERBILT 579, 365, 389, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1384-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 3MM(H) Reference Number: IEHA563
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1381-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 7.5MM(P) X 4MM(H) Reference Number: IEHA474
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1383-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 4MM(H) Reference Number: IEHA554
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1372-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 3MM(H) Reference Number: IEHA443
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1373-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H) Reference Number: IEHA444
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V128000·2020-03-04

    Horton Ambulances Recalled for Electrical Short Circuit Risk

    Halcore Group is recalling 2016-2019 Horton Type I and III ambulances because an undersized A/C power cord may cause an electrical short circuit, increasing the risk of fire or shock.

    Product
    HORTON — HORTON TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1369-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Misalignment

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation or margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 3MM(H) Reference Number: IEHA353
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1356-2020·2020-03-04

    Zimmer Sterile Disposable Tourniquet Cuff Recalled for Bladder Leak

    Zimmer Surgical Inc is recalling 58 units of sterile tourniquet cuffs because a leak between bladders may cause both to inflate or deflate simultaneously.

    Product
    Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1374-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Fit Issues

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 6MM(H) Reference Number: IEHA446
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1352-2020·2020-03-04

    Breas Medical Recalls Vivo Ventilator Protective Covers Due to Obstruction Risk

    Breas Medical is recalling 629 Vivo ventilator protective covers because the design may obstruct the exhalation valve control pressure tube.

    Product
    Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the Vivo 50 and Vivo 65 ventilators - Product Usage: The protective cover is intended for additional protection of the Vivo 50, Vivo 55, Vivo 60 and Vivo 65…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1370-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 4MM(H) Reference Number: IEHA354
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 3MM(H) Reference Number: IEHA463
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0750-2020·2020-03-04

    Domino Foods Recalls SYSCO Brown Sugar Due to Foreign Material

    Domino Foods is recalling SYSCO Classic Light Brown Cane Sugar because it may contain foreign material. The product was distributed to 23 states and Saudi Arabia.

    Product
    SYSCO Classic Light Brown Cane Sugar, 25 LB bag, UPC 074865990301, Lots 50043 (Best By Jan 22, 2022) & 50045 (Best By Jan 24, 2022)
    Category
    Food
    Distribution
    23 states