The Recall Desk

State

South Carolina product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39776–39800 of 80959

  • HighFDA (Food)·F-0376-2019·2018-11-14

    Request Foods Recalls Evol Portabello Goat Cheese Ravioli for Contamination Risk

    Request Foods Incorporated is recalling Evol Portabello Goat Cheese Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Evol Portabello Goat Cheese Ravioli 18oz UPC 91627 00789 Frozen 6, 18oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0390-2019·2018-11-14

    Cordis POWERFLEX PRO PTA Dilatation Catheter Recalled for Burst Strength Failure

    Cordis Corporation is recalling 162 units of POWERFLEX PRO PTA Dilatation Catheters because they may not meet internal manufacturing burst strength specifications.

    Product
    Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0397-2019·2018-11-14

    Zimmer Biomet Recalls RapidFlap SpinDown Clamp Due to Assembly Error

    Zimmer Biomet is recalling 3,246 RapidFlap SpinDown Clamps because the nut was assembled incorrectly. The device is used to re-attach bone flaps after craniotomy.

    Product
    Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Ref Number: 75-1040 Used for the re-attachment of the bone flap after a craniotomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0232-2019·2018-11-14

    Recall of Testosterone 12.5mg Pellet due to Sterility Concerns

    Qualgen, LLC is recalling Testosterone 12.5mg pellets nationwide because the sterility of the product cannot be assured. Consumers should stop using the affected lots and contact the manufacturer or pharmacist.

    Product
    Testosterone 12.5mg pellet, 1 count (NDC 69761-112-01), 6 count (NDC 69761-112-06), 12 count (NDC 69761-112-12), and 30 count (NDC 69761-112-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0388-2019·2018-11-14

    Kashi Mayan Harvest Bake Bowl Recalled for Listeria and Salmonella Risk

    Request Foods Incorporated is recalling Kashi Mayan Harvest Bake Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Kashi, Mayan Harvest Bake Bowl 10oz. UPC 18627 10605 Frozen 8, 10oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0391-2019·2018-11-14

    Request Foods Recalls Kashi Coconut Lemongrass Rice Bowls Due to Contamination Risk

    Request Foods Incorporated is recalling Kashi Coconut Lemongrass Rice Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Kashi, Coconut Lemongrass Rice Bowl 9oz. UPC 18627 10765 Frozen 8, 9oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0234-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 25 mg pellets nationwide because the company lacks assurance of sterility for these products.

    Product
    Testosterone 25 mg pellet, 1 count (NDC: 69761-125-01) and 30 count vials (NDC: 69761-125-30), Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0397-2019·2018-11-14

    Request Foods Recalls Curry Jackfruit Bowls Due to Listeria and Salmonella Risk

    Request Foods Incorporated is recalling The Jackfruit Company Curry Jackfruit Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    The Jackfruit Company Curry Jackfruit Bowl 9oz. UPC 59806 00344 Frozen 6, 9oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0392-2019·2018-11-14

    Kashi Creamy Cashew Noodle Bowl Recalled for Listeria and Salmonella Risk

    Request Foods Incorporated is recalling Kashi Creamy Cashew Noodle Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Kashi, Creamy Cashew Noodle Bowl 8oz. UPC 18627 10767 Frozen 8, 8oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0400-2019·2018-11-14

    Request Foods Recalls Beecher's Mariachi Mac & Cheese Due to Contamination Risk

    Request Foods Incorporated is recalling Beecher's Mariachi Mac & Cheese because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Beecher's Mariachi Mac & Cheese 20oz. UPC 82045 11274 Frozen 8, 20oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2019·2018-11-14

    Request Foods Recalls Evol Butternut Squash & Sage Ravioli

    Request Foods Incorporated is recalling Evol Butternut Squash & Sage Ravioli due to possible contamination with Listeria monocytogenes and Salmonella.

    Product
    Evol Butternut Squash & Sage Ravioli 8oz. UPC 98997 80974 Frozen 6, 8oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0235-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 37.5 mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 37.5 mg pellet, 1 count (NDC 69761-137-01), 6 count (NDC 69761-137-06), 12 count (NDC 69761-137-12) and 30 count (NDC 69761-137-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0396-2019·2018-11-14

    Zimmer Biomet Recalls RapidFlap SpinDown Clamps Due to Assembly Error

    Zimmer Biomet is recalling 11,580 RapidFlap SpinDown Clamps because the nut was assembled incorrectly. The devices are used to re-attach bone flaps after craniotomy.

    Product
    Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the re-attachment of the bone flap after a craniotomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0231-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 100mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 100mg pellet, 1 count (NDC 69761-110-01), 6 count (NDC 69761-110-06), 12 count (NDC 69761-110-12), and 30 count (NDC 69761-110-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0384-2019·2018-11-14

    BD Nexiva IV Catheter Recall Due to Needle Shield Failure

    Becton Dickinson is recalling 133,230 units of BD Nexiva Closed IV Catheter Systems because a needle shield defect may increase the risk of contaminated needlestick injuries.

    Product
    BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage: BD Nexiva Closed IV Catheter System Dual Port (hereafter referred to as BD Nexiva device or catheter) (see Figure below) incorporates a passive needle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0386-2019·2018-11-14

    Request Foods Recalls Kashi Sweet Potato Quinoa Bowls for Contamination

    Request Foods Incorporated is recalling Kashi Sweet Potato Quinoa Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Kashi, Sweet Potato Quinoa Bowl 9oz. UPC 18627 10547 Frozen 8, 9oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0404-2019·2018-11-14

    Request Foods Recalls Vegetable Egg & Cheese Frittata for Listeria and Salmonella

    Request Foods Incorporated is recalling specific lots of Gordon Choice Vegetable Egg & Cheese Frittata due to possible contamination with Listeria monocytogenes and Salmonella.

    Product
    Gordon Choice / GFS Vegetable Egg & Cheese Frittata 60oz. UPC 93901 19112 Frozen 4 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0401-2019·2018-11-14

    Request Foods Recalls Beecher's Enchilada Bowls Due to Contamination Risk

    Request Foods Incorporated is recalling Beecher's Enchilada Bowl Blanco frozen units because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    Beecher's Enchilada Bowl Blanco 9oz. UPC 82045 11381 Frozen 8, 9oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0398-2019·2018-11-14

    Request Foods Recalls Jackfruit Bowls Due to Listeria and Salmonella Risk

    Request Foods Incorporated is recalling The Jackfruit Company Enchilada Jackfruit Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.

    Product
    The Jackfruit Company Enchilada Jackfruit Bowl 9.5oz. UPC 59806 00341 Frozen 6, 9.5oz. units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0409-2019·2018-11-14

    Siemens Dimension Thermal Chamber Motor Cable Recall for Insulation Defect

    Siemens is recalling 277 Dimension thermal chamber motor cables worldwide due to single insulation instead of required double insulation, posing a potential electrical shock risk.

    Product
    Dimension Thermal Chamber Motor Cable located in the following models: Model/UDI Number: Dimension¿ EXL 200 00630414593579; Dimension¿ EXL with LM 00630414593500; Dimension¿ EXL with LM with STM 00630414593593; Dimension¿ RxL Max 00630414949789; Dimension¿ RxL Max HM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0393-2019·2018-11-14

    Zimmer Biomet Recalls RapidFlap SpinDown Clamp Due to Assembly Error

    Zimmer Biomet is recalling 12,825 units of the RapidFlap System 12mm SpinDown Clamp because the nut was assembled incorrectly. The defect affects sterile clamps used for craniotomy bone flap re-attachment.

    Product
    Biomet Microfixation RapidFlap System 12mm SpinDown Clamp, sterile Ref Number: 75-1020 Used for the re-attachment of the bone flap after a craniotomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0228-2019·2018-11-14

    Qualgen Recalls Estradiol Pellets Due to Sterility Assurance Concerns

    Qualgen, LLC is recalling Estradiol 18mg pellets because the company cannot assure the sterility of the product. The recall covers specific vial sizes distributed nationwide.

    Product
    Estradiol 18mg pellet, 1 count (NDC 69761-018-01), 6 count (NDC 69761-018-06), 12 count (NDC 69761-018-12), and 30 count (NDC 69761-018-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0387-2019·2018-11-14

    Becton Dickinson Recalls PCEA Administration Sets Due to Potential Leaks

    Becton Dickinson is recalling PCEA Administration Sets because they may leak at the connection point. The recall covers 566,737 units distributed worldwide.

    Product
    PCEA Kit ASV Yellow Stripe Microbore, Catalog Number 10800177 Product Usage: PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve. Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set.…
    Category
    Medical Device
    Distribution
    Distributed nationwide