The Recall Desk

State

South Carolina product recalls

73,833 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.

Which agencies issued them

These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54951–54975 of 80986

  • SevereFDA (Devices)·Z-1060-2016·2016-03-16

    Arrow UltraFlex IAB Recall for Potential Sheath Separation and Bleeding Risk

    Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    UltraFlex IAB: 7.5Fr 40cc; Product Code: IAB-06840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0759-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine Sulfate Syringes for Sterility Concerns

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate 11 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Morphine Sulfate 11 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0911-2016·2016-03-16

    Abbott Vascular Recalls MitraClip Clip Delivery System Due to Mandrel Fracture

    Abbott Vascular is recalling the MitraClip Clip Delivery System because a mandrel fracture may prevent the clip from detaching during implantation.

    Product
    MitraClip Clip Delivery System, product number MSK0101. The MitraClip System contains the Clip Delivery System, product number CDS0201, GTIN 08717648195914 and the Steerable Guide Catheter, product number SGC0101, GTIN 08717648195921. The MitraClip Clip Delivery System (CDS)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0740-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Baclofen Syringes

    Hartley Medical Center Pharmacy is recalling specific hydromorphone and baclofen syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone 12 mg/ml/Baclofen 450 mcg/ml, vol. 20 ml, syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0763-2016·2016-03-16

    Morphine Sulfate Syringes Recalled for Lack of Sterility Assurance

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate 0.5 mg/ml syringes due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 0.5 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0746-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling Hydromorphone HCL and Bupivacaine HCL syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone HCL 10 mg/ml/Bupivacaine HCL 30 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0751-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Fentanyl Syringes

    Hartley Medical Center Pharmacy is recalling specific hydromorphone and fentanyl syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone HCL 10 mg/ml/Fentanyl Citrate 0.15 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0744-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine HCL syringes due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 20 mg/ml/Bupivacaine HCL 11.3 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0752-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone Syringes Due to Sterility Concerns

    Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Hydromorphone HCL 10 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1062-2016·2016-03-16

    Arrow Percutaneous Insertion Tray Recalled for Potential Sheath Separation

    Arrow International is recalling specific Percutaneous Insertion Trays because the sheath body may separate from the hub, posing a risk of bleeding.

    Product
    Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0765-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Sufentanil Citrate Syringes Due to Sterility Concerns

    Hartley Medical Center Pharmacy is recalling Sufentanil Citrate/Clonidine/Bupivacaine syringes because the agency could not ensure the product was sterile.

    Product
    Sufentanil Cit 50 mcg/ml/Clonidine HCL 1 mcg/ml/Bupivacaine HCL 5 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1047-2016·2016-03-16

    Gi Supply Recalls Large Volume Paracentesis Kits Due to Missing Clamp

    Gi Supply is recalling Large Volume Paracentesis Kits because the pinch clamp on the RP Bag may be missing, posing a splash hazard to users.

    Product
    Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most components. Packed sterile in Tyvek bag. Catalog #: GIS-28 Lot #: 61442434 Expiration Date: 2018/04
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Drugs)·D-0741-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine Sulfate Combination Vials

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 9 mg/ml/Sufentanil Cit 180 mcg/ml/Bupivacaine HCL 33 mg/ml, vol. 20 ml vial, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1068-2016·2016-03-16

    Bard Denali Filter Delivery System Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2016·2016-03-16

    Philips Respironics Recalls Trilogy and Garbin Ventilators Due to Software Issue

    Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.

    Product
    Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2016·2016-03-16

    Sedecal Mobile X-ray Systems Recalled for Uncommanded Movements

    Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.

    Product
    Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist on both adult and pediatric patients for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16122·2016-03-16

    SRAM Recalls Zipp Bicycle Wheel Hubs Due to Crash and Injury Hazards

    SRAM is recalling Zipp 88 aluminum front hubs because the flanges can fail, posing a crash and injury hazard. Consumers should stop using the hubs and contact SRAM for a free replacement.

    Product
    Zipp 88 aluminum front hubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1064-2016·2016-03-16

    Arrow Recalls Percutaneous Sheath Introducer Sets Due to Packaging Damage

    Arrow International Inc. is recalling Super Arrow-Flex Percutaneous Sheath Introducer Sets because packaging damage may compromise sterility, posing a potential infection risk.

    Product
    Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex Percutaneous Sheath Introducer Set with Integral Hemostasis Valve/Side Port and Radiopaque Tip Marker Band Contents: 1: . . . . . . . . . Sheath*: ***…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V154000·2016-03-16

    Terex Recalls Aerial Devices Due to Suspension Air Bag Defect

    Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.

    Product
    TEREX — TEREX TM125, HRX, C5000, C6000
    Category
    Vehicle
    Distribution
    Distributed nationwide