The Recall Desk

State

South Carolina product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33351–33375 of 80890

  • SevereNHTSA·20V049000·2020-01-29

    Forest River Recalls 2020 Recreational Trailers Due to Brake Switch Failure

    Forest River is recalling 218 units of 2020 recreational trailers because a failed break-away switch may prevent brakes from engaging if the trailer separates from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER FREEDOM EXPRESS, WILDCAT MAXX, WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0796-2020·2020-01-29

    Preferred Pharmaceuticals Recalls Ranitidine Tablets Due to NDMA Impurity

    Preferred Pharmaceuticals is recalling 150 mg Ranitidine tablets because of detected NDMA impurity. The affected products were distributed to physicians in seven states.

    Product
    Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 150 mg, a) 30 count bottles (NDC: 68788-7388-3), b) 60 count bottles (NDC: 68788-7388-6), c) 90 count bottles (NDC: 68788-7388-9), d) 100 count bottles (NDC: 68788-7388-1)
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0797-2020·2020-01-29

    Preferred Pharmaceuticals Recalls Ranitidine Tablets Due to NDMA Impurity

    Preferred Pharmaceuticals is recalling Ranitidine Tablets, 300 mg, because the presence of the NDMA impurity was detected in the product.

    Product
    Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 300 mg, Rx Only, a) 14 count bottles (NDC: 68788-6382-1), b) 30 count bottles (NDC: 68788-6382-3), c) 90 count bottles (NDC: 68788-6382-9), d) 100 count bottles (NDC: 68788-6382-0)
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0795-2020·2020-01-29

    Denton Pharma Recalls Ranitidine Tablets Due to NDMA Impurity

    Denton Pharma is recalling 467 bottles of Ranitidine Tablets 300 mg because of the presence of NDMA impurity. The affected products were distributed nationwide.

    Product
    Ranitidine Tablets, USP 300 mg a). 15-count bottles (NDC 70934-287-15), b). 90-count bottles (NDC 70934-287-90), Rx Only, Repackaged by: Northwind Pharmaceuticals North Brenheim, NY 12131
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V050000·2020-01-29

    Vactor 2100i Vehicles Recalled for Safety Interlock Software Defect

    Vactor is recalling 2017-2020 2100i vehicles because a software defect may cause safety interlocks to fail, leading to unintentional vehicle movement and increased crash risk.

    Product
    VACTOR — VACTOR 2100I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0830-2020·2020-01-29

    Siemens ADVIA Centaur Folate Test Kits Recalled for Potential Interference

    Siemens is recalling ADVIA Centaur Folate test kits because homocysteine assays may cause elevated folate results.

    Product
    Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate in serum or red blood cells SMN: 10325366
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0553-2020·2020-01-29

    Morrison's Cornbread Dressing Recalled for Listeria Risk

    Savannah Food Company is recalling Morrison's cornbread dressing because eggs used in manufacturing may be contaminated with Listeria monocytogenes.

    Product
    Morrison's cornbread dressing packaged in 4lb tray
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0832-2020·2020-01-29

    PTS Diagnostics CardioChek Plus Analyzer Recalled for Battery Overheating Risk

    Polymer Technology Systems is recalling 44,448 CardioChek Plus Professional Analyzers because a battery terminal defect can cause overheating if batteries are inserted incorrectly.

    Product
    PTS Diagnostics CardioChek Plus Professional Analyzer, New analyzer, boxed, with carrying case, Reference Numbers 2700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V051000·2020-01-29

    KME Predator Emergency Vehicles Recalled for Flashlight Battery Explosion Risk

    Kovatch Mobile Equipment is recalling specific KME Predator emergency vehicles because flashlight battery packs may explode while charging, increasing injury risk.

    Product
    KME — KME PREDATOR SS PUMPER, PREDATOR SS TDA, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20059·2020-01-29

    Summer Infant Recalls SwaddleMe Inclined Sleepers Due to Suffocation Risk

    Summer Infant is recalling about 46,300 SwaddleMe By Your Bed inclined sleepers to prevent the risk of infant suffocation. Consumers should stop using the product immediately and contact the company for a refund.

    Product
    SwaddleMe By Your Bed Sleeper inclined sleeper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0833-2020·2020-01-29

    PTS Diagnostics CardioChek Plus Analyzer Recalled for Battery Overheating Risk

    Polymer Technology Systems is recalling 44,448 refurbished CardioChek Plus Professional Analyzers because a battery terminal defect may cause overheating if batteries are inserted incorrectly.

    Product
    PTS Diagnostics CardioChek Plus Professional Analyzer, Refurbished analyzer, without box or carrying case, Reference Numbers 2702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0843-2020·2020-01-29

    Beckman Coulter Recalls iChem VELOCITY Urine Chemistry Analyzers

    Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Analyzers because a software issue may prevent specific gravity flags, potentially leading to erroneous test results.

    Product
    iChem VELOCITY Urine Chemistry Analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0819-2020·2020-01-29

    GE Healthcare Recalls Centricity Universal Viewer 6.0 for Measurement Errors

    GE Healthcare is recalling Centricity Universal Viewer 6.0 because incorrect measurements in DICOM files may lead to potential misdiagnosis.

    Product
    Centricity Universal Viewer 6.0, a device that displays medical images and data from various imaging sources, and from other healthcare information sources.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0557-2020·2020-01-29

    Savannah Classics Bread Stuffing Recalled for Listeria Risk

    Savannah Food Company is recalling Savannah Classics Classic Bread Stuffing because eggs used in manufacturing may be contaminated with Listeria monocytogenes.

    Product
    Savannah Classics Classic Bread Stuffing packaged in 4.5lb trays
    Category
    Food
    Distribution
    9 states
  • HighCPSC·20061·2020-01-29

    Delta Recalls Incline Sleepers for Newborns Due to Suffocation Risk

    Delta Enterprise Corp. is recalling about 5,900 incline sleepers for newborns to prevent the risk of suffocation. Consumers should stop using the products immediately.

    Product
    Beautyrest Beginnings Incline Sleeper with Adjustable Feeding Position for Newborns; Disney Baby Minnie Mouse Incline Sleeper with Adjustable Feeding Position for Newborns; Delta Children Deluxe 3-in-1 Activity Rocker, Feeder and Sleeper; Simmons Kids Beautyrest Deluxe 3-in-1…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0556-2020·2020-01-29

    Savannah Classics Cornbread Dressing Recalled for Listeria Risk

    Savannah Food Company is recalling Savannah Classics Classic Cornbread Dressing because eggs used in manufacturing may be contaminated with Listeria monocytogenes.

    Product
    Savannah Classics Classic Cornbread Dressing packaged in 7lb trays
    Category
    Food
    Distribution
    9 states
  • HighCPSC·20062·2020-01-29

    Graco Recalls Little Lounger Rocking Seats to Prevent Suffocation Risk

    Graco is recalling Little Lounger Rocking Seats to prevent the risk of infant suffocation. Consumers should stop using the product and contact Graco for a refund.

    Product
    Graco Little Lounger Rocking Seat
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0555-2020·2020-01-29

    Savannah Classics Cornbread Dressing Recalled for Listeria Risk

    Savannah Food Company is recalling Savannah Classics Special Cornbread Dressing because eggs used in manufacturing may be contaminated with Listeria monocytogenes.

    Product
    Savannah Classics Special Cornbread Dressing packaged in 7lb trays
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0554-2020·2020-01-29

    Morrison's Cornbread Dressing Recalled for Listeria Risk

    Savannah Food Company is recalling Morrison's cornbread dressing because eggs used in manufacturing may be contaminated with Listeria monocytogenes.

    Product
    Morrison's cornbread dressing packaged in 7lb trays
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0836-2020·2020-01-29

    Paltop Dental Implant Recall Due to Incorrect Cover Screw Packaging

    Paltop Advanced Dental Solutions is recalling 67 dental implants because some were packaged with the wrong cover screw, preventing proper fit.

    Product
    Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0828-2020·2020-01-29

    Medicrea Pass LP Blunt K-wire Recalled for Incompatibility with Screws

    Medicrea International is recalling 190 units of Pass LP Blunt K-wires because they may not fit into Conical Cannulated Screws.

    Product
    Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
    Category
    Medical Device
    Distribution
    Distributed nationwide