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.

Which agencies issued them

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.

32926–32950 of 80889

  • SevereFDA (Devices)·Z-1167-2020·2020-02-19

    Pacific Medical Ultrasound Transducers Recalled for Non-OEM Component Use

    Pacific Medical Group is recalling 5,897 ultrasound transducers serviced with unverified non-OEM components, which may cause inaccurate monitoring or patient burns.

    Product
    Ultrasound Transducer (M2736A), that may have been serviced with the following: Pacific Medical Philips Avalon Smart US/TOCO Cable Assembly, NFPHA9020; Pacific Medical Philips M2736A Avalon Smart Ultrasound Bottom Case, NFPHA9515
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1183-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Combined Spinal Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Combined Spinal Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1212-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Drugs)·D-0839-2020·2020-02-19

    Akorn Recalls Subpotent Hydrocortisone and Acetic Acid Otic Solution

    Akorn Inc is recalling 16,078 bottles of Hydrocortisone and Acetic Acid Otic Solution due to low assay results for the hydrocortisone component.

    Product
    Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701; NDC 50383-901-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0930-2020·2020-02-19

    Tytek Medical Recalls PneumoDart Devices Due to Occluded Needle Defect

    Tytek Medical Inc is recalling 3,565 PneumoDart devices because a defect involving an occluded needle was discovered during a training exercise.

    Product
    PneumoDart, 14 ga x 3.25in., REF TM-317 A compact, sterile, device intended for the introduction into the body to facilitate the removal of air from the pleural cavity as a result of a tension pneumothorax condition.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0845-2020·2020-02-19

    Efficient Laboratories Recalls Rompe Pecho CF Cold & Flu Due to Microbial Contamination

    Efficient Laboratories is recalling 5,249 bottles of Rompe Pecho CF Cold & Flu with Honey due to microbial contamination. The product was distributed nationwide in the USA.

    Product
    Rompe Pecho CF Cold & Flu with Honey, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166.UPC 0 00856 33106 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1179-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05400-CA1
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1112-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidifier Nebulizer Kits

    Teleflex Medical is recalling 30,566 Hudson RCI Comfort Flo humidifier nebulizer kits because water may flood the column and enter the circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Corrugated Humidification System, REF 2415, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1172-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1117-2020·2020-02-19

    Teleflex Recalls Rusch Greenlite Laryngoscope Blades Due to Breakage Reports

    Teleflex Medical Inc. is recalling Rusch Greenlite Single-Use Metal Laryngoscope Blades because they may break at a welded joint during setup or use.

    Product
    Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1163-2020·2020-02-19

    Pacific Medical External Toco Transducers Recalled for Unverified Components

    Pacific Medical Group is recalling 1,603 External Toco Transducers serviced with non-OEM parts that were not appropriately verified or validated.

    Product
    External Toco Transducer (M1355A), that may have been serviced with the following: Pacific Medical Philips M1355A Toco Bottom Case, NFPH9315; Pacific Medical Philips M1355A Toco Cable Assembly, NFPH9320; Pacific Medical Philips M1355A Toco Gauge, NFPH9340
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1113-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidification Systems

    Teleflex Medical is recalling 60,467 Hudson RCI Comfort Flo Corrugated Humidification Systems because water may flood the column and enter the circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote Temperature Port, REF 2416, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1168-2020·2020-02-19

    Pacific Medical Toco MP Transducers Recalled for Non-OEM Components

    Pacific Medical Group Inc. is recalling Toco MP Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal monitoring and patient burns.

    Product
    Toco MP Transducer (M2734B), that may have been serviced with the following: Pacific Medical Philips M2734B Avalon Smart TOCO Bottom Case, NFPHA9315-B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1213-2020·2020-02-19

    Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk

    Arrow International is recalling 343,105 Epidural Catheterization Kits with FlexTip Plus Catheters because the included loss of resistance syringes may fail, potentially causing dural puncture.

    Product
    Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1176-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1209-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Sets

    Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1166-2020·2020-02-19

    Pacific Medical Toco+ Transducers Recalled for Unverified Service Components

    Pacific Medical Group is recalling 2,170 Toco+ transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal/maternal monitoring and patient burns.

    Product
    Toco+ transducer with ECG/IUP capability (wired), that may have been serviced with the following: Pacific Medical Philips Avalon Smart US/TOCO Cable Assembly, NFPHA9020; Pacific Medical Philips Avalon Smart M2734A/2735A Toco Gauge Flex, NFPHA9341
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1174-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1196-2020·2020-02-19

    Arrow International Recalls Pediatric Epidural Catheterization Sets Due to Syringe Failure Risk

    Arrow International is recalling FlexTip Plus Epidural Catheterization Sets for pediatric lumbar placement because the included loss of resistance syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement, Product Code EC-05520-P
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1205-2020·2020-02-19

    Arrow International Recalls 10 cc Luer-Slip Loss of Resistance Syringes

    Arrow International Inc is recalling 10 cc Luer-Slip Loss of Resistance Syringes due to potential failures that could result in dural puncture.

    Product
    10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Drugs)·D-0846-2020·2020-02-19

    Rompe Pecho EX Expectorant Recalled for Microbial Contamination

    Efficient Laboratories, Inc. is recalling 5,387 bottles of Rompe Pecho EX Expectorant due to microbial contamination. Consumers should stop using the product and return it to the place of purchase.

    Product
    Rompe Pecho EX Expectorant, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 30106 1
    Category
    Drug
    Distribution
    Distributed nationwide