The Recall Desk

State

South Carolina product recalls

73,824 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.

These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49526–49550 of 80977

  • SevereFDA (Food)·F-1194-2017·2017-01-18

    All American Seasonings Recalls Non-GMO Sour Cream and Onion Seasoning

    All American Seasonings is recalling 428 bags of Non-GMO Sour Cream & Onion seasoning due to potential Salmonella contamination.

    Product
    Non-GMO Sour Cream & Onion / Deep River Snacks. Product Code: T3527. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1200-2017·2017-01-18

    All American Seasonings Recalls Kay's Naturals Cheese Puff Seasoning

    All American Seasonings is recalling 80 bags of Kay's Naturals Cheese Puff Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Cheese Puff Seasoning / Kay's Naturals. Product Code: T3852. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1227-2017·2017-01-18

    St. Clair Pistachio Cream Recalled for Salmonella Risk

    St. Clair Foods is recalling Pistachio Cream products due to potential salmonella contamination from an ingredient.

    Product
    Pistachio Cream, packaged under the following brands: (a) St. Clair, product code 104004, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114004 (b) Ron's Home Style Foods, product code 900603, NET WT. 5 LBS(2.27 kg), DIST. BY RON'S HOME STYLE FOODS…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1234-2017·2017-01-18

    Fourth Street Barbecue Recalls Macaroni and Cheese Due to Salmonella Risk

    Fourth Street Barbecue is voluntarily recalling specific macaroni and cheese products because the powdered cheese packets may contain milk powder contaminated with Salmonella.

    Product
    Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320; Double Takes: Best By: 10/11/17 10/12/17 10/13/17 10/19/17 10/20/17 10/24/17 11/28/17 11/29/17 11/30/17; UPC: 63927701208:
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0964-2017·2017-01-18

    Stryker Recalls Reprocessed Electrophysiology Catheter Cables Due to Sterility Breach

    Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.

    Product
    Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT, D134401, CB3410CT, CB3412CT Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0430-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1252-2017·2017-01-18

    Roy Roger's Pancake Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Roy Roger's Pancake Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Roy Roger's Pancake Mix, Net Wt., 2 lb. 8 oz. bags, UPC Code 0 73484 22724 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0967-2017·2017-01-18

    C.R. Bard Recalls Medical Devices Containing Latex Catheters

    C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.

    Product
    SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2017·2017-01-18

    Brand Castle Monkey Bread Mix Recalled for Salmonella

    Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.

    Product
    In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY BRAND CASTLE, LLC BEDFORD HTS, OH 44146 www.brandcastle.com UPC 8 44527 03278 2
    Category
    Food
    Distribution
    38 states
  • HighFDA (Food)·F-1247-2017·2017-01-18

    House-Autry Buttermilk Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buttermilk Biscuit Mix because it contains milk from a supplier recalling product due to possible Salmonella.

    Product
    House-Autry Buttermilk Biscuit Mix Tote, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15500 9,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1249-2017·2017-01-18

    House-Autry Butterflake Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling 606 bags of Butterflake Biscuit Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House-Autry Butterflake Biscuit Mix, Net Wt. 25 lb. bags, UPC Code 0 73484 20513 1,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1250-2017·2017-01-18

    Buddy's Bar-B-Q Hushpuppy Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buddy's Bar-B-Q Hushpuppy Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Buddy's Bar-B-Q Hushpuppy Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22156 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1235-2017·2017-01-18

    Cheese Club Mac and Cheese Recalled for Salmonella Risk

    Fourth Street Barbecue is recalling Cheese Club mac and cheese products because milk powder ingredients may be contaminated with Salmonella.

    Product
    Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0963-2017·2017-01-18

    Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns

    Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.

    Product
    Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1248-2017·2017-01-18

    House-Autry Cheese Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Cheese Biscuit Mix because it contains milk from a supplier recalling product for possible Salmonella.

    Product
    House-Autry Cheese Biscuit Mix, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15510 8,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide