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.

55651–55675 of 80986

  • HighFDA (Devices)·Z-0686-2016·2016-01-27

    Abeon Wilson Penile Implantation System Retractor Frame Recalled for Sterility Compromise

    Abeon Medical Corporation is recalling Wilson Penile Implantation System Retractor Frames because some sealed pouches contain tears that compromise the product's sterility.

    Product
    Wilson Penile Implantation System Retractor Frame, Retractor Stays & Penile Elevation Strap, SINGLE USE ONLY Rx ONLY. Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0683-2016·2016-01-27

    IBA Dosimetry Lift Table Recalled for Uncontrolled Movement Risk

    IBA Dosimetry GmbH is recalling Lift Table Type 4320 units because they may move up in an uncontrolled manner when connected to power.

    Product
    IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0682-2016·2016-01-27

    GE Medical Systems Recalls Anesthesia Device Service Kits Due to Valve Defect

    GE Medical Systems is recalling 240 anesthesia device service kits because a drive gas check valve could become stuck open, potentially causing excessive pressure in the patient breathing circuit.

    Product
    Anesthesia device service kits. ASSY-MSN, VENT ENGINE ASSY, 1503-8101-000 ASSY-MSN, VENT ENGINE ASSY 7900, 1009-8216-000 ASSY-MSN, VENT ENGINE ASSY AESPIRE 7900 1009-8423-000 ASSY-MSN, VENT ENGINE ASSY, AESTIVA 7900 MRI 1503-8102-000 ASSY-MSN, VLV ASSY DR GAS CHK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0664-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Arm Sleeves Due to Overheating Risk

    MWT Materials, Inc. is recalling 31 Accusorb MRI arm sleeves distributed in New York and Massachusetts because they may overheat and injure patients when not used correctly.

    Product
    Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0675-2016·2016-01-27

    Rymed InVision-Plus IV Connectors Recalled for Cracking Risk

    Rymed Technologies is recalling InVision-Plus IV connectors because the female luer component may crack during use.

    Product
    InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0673-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Shielding Blankets Due to Overheating Risk

    MWT Materials, Inc. is recalling Accusorb MRI MAC7030 shielding blankets and covers because they may overheat and cause patient injury when not used correctly.

    Product
    Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0583-2016·2016-01-27

    Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Microdroplets

    Pine Pharmaceuticals is recalling specific lots of Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.

    Product
    Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16724·2016-01-27

    Lunera Recalls Helen GX23 LED Lamps Due to Fire and Shock Hazards

    Lunera is recalling approximately 60,000 Helen GX23 LED lamps because they can overheat, posing fire, burn, and electric shock hazards. No injuries have been reported.

    Product
    Helen GX23 LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0668-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Radio Frequency Shielding Blankets

    MWT Materials, Inc. is recalling 14 Accusorb MRI radio frequency shielding blankets and body-part covers because they may overheat and lead to patient injury when not used correctly.

    Product
    Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and MRI-03 L (Lower) Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0678-2016·2016-01-27

    GE Healthcare Aestiva 7900 Ventilator Recall for Stuck Valve Risk

    GE Medical Systems is recalling two Aestiva 7900 ventilators because a stuck valve could cause excessive pressure and barotrauma.

    Product
    GE Healthcare, Aestiva 7900, 1006-9305-000. This version of the Datex-Ohmeda 7900 ventilator is used in Datex-Ohmeda Aestiva/5 anesthesia systems. It is a microprocessor based, electronically controlled, pneumatically driven ventilator that provides patient ventilation during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0679-2016·2016-01-27

    GE Healthcare Aestiva MRI Ventilator Recalled for Valve Defect

    GE Medical Systems is recalling 84 Aestiva MRI anesthesia systems because a drive gas check valve may become stuck open, potentially causing excessive pressure in the patient breathing circuit.

    Product
    GE Healthcare, Aestiva MRI, 1006-9310-000. This version of the Datex-Ohmeda 7900 ventilator is used in Datex-Ohmeda Aestiva/5 anesthesia systems. It is a microprocessor based, electronically controlled, pneumatically driven ventilator that provides patient ventilation during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0573-2016·2016-01-27

    Freedom Pharmaceuticals Recalls Baclofen Powder Due to Foreign Substance

    Freedom Pharmaceuticals is recalling specific lots of Baclofen USP powder because of the presence of a foreign substance.

    Product
    Baclofen USP powder, packaged in (a) 25gm (4 oz container), (b) 100gm (16 oz container), (c) 500 gm (70 oz container), and (d) 1000 gm (120 oz container, Rx only, 801 W New Orleans St. Broken Arrow, OK 74011. NDC: (a) 52372-0909-25; (b) 52372-0909-01; (c) 52372-0909-50; (d)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0670-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Large Torso Wrap Due to Overheating Risk

    MWT Materials, Inc. is recalling five units of Accusorb MRI Large Torso Wraps because they may overheat when not used correctly, posing a risk of patient injury.

    Product
    Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large Torso Wrap Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0681-2016·2016-01-27

    GE Healthcare Anesthesia Systems Recalled for Potential Barotrauma Risk

    GE Medical Systems is recalling certain Aisys and Avance anesthesia systems because a stuck valve could cause excessive pressure in the patient breathing circuit, potentially leading to barotrauma.

    Product
    GE Healthcare, Aisys CS2,1011-9050-000; Avance Amingo,1009-9002-000, & Avance CS2, 1009-9050-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0578-2016·2016-01-27

    Grato Holdings Recalls Energique Shingles Pain Spray Due to Microbial Contamination

    Grato Holdings is recalling Energique Shingles Pain & Ulceration Relief Topical Spray due to out-of-specification microbial counts. The recall covers 371 bottles distributed nationwide and to Guatemala and Canada.

    Product
    Energique, Homeopathic Remedy, Shingles Pain & Ulceration Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0137-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Shingles Pain & Ulceration Relief Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0571-2016·2016-01-27

    Morton Grove Recalls Lindane Lotion Due to Out-of-Specification Assay

    Morton Grove Pharmaceuticals is recalling specific lots of Lindane Lotion because stability samples failed assay testing. Consumers should stop using the product and return it to their pharmacy.

    Product
    Lindane Lotion, USP 1%, For External use Only, Rx Only, 2 fl oz (60 mL) bottle, MGP, NDC 60432-833-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0576-2016·2016-01-27

    Energique Homeopathic Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique homeopathic topical spray due to out-of-specification microbial counts. The product was distributed nationwide and to Canada and Guatemala.

    Product
    Energique, Homeopathic Remedy, Muscle/Tendon Pain & Stress Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0132-1, Dist. by Energique, Inc. Woodbine, IA 51579; ALSO LABELED AS --- Liddell Laboratories, Muscle/Tendon Pain & Stress Relief, Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0579-2016·2016-01-27

    Energique Headache Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique Headache Pain & Sinus Pressure Relief Topical Spray due to microbial contamination.

    Product
    Energique, Homeopathic Remedy, Headache Pain & Sinus Pressure Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0134-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Headache Pain & Sinus Pressure Relief, Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0674-2016·2016-01-27

    Valeant SPAG-2 Nebulizer Recalled for Incorrect Serial Labels and Manual Information

    Valeant is recalling 1,178 SPAG-2 nebulizer units because serial ID labels and operation manuals contain incorrect or outdated information.

    Product
    Valeant Pharmaceuticals North America, Small Particle Size Aerosol Generator, SPAG-2 6000 series. Model No. SPAG-2. A nebulizer pneumatic flow system for the administration of Virazole (ribavirin) aerosol.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0574-2016·2016-01-27

    PD-Rx Recalls Phentermine Hydrochloride Capsules Due to Impurity Failures

    PD-Rx Pharmaceuticals is recalling 1,685 bottles of Phentermine Hydrochloride capsules because stability tests showed impurities exceeded specifications.

    Product
    PHENTERMINE HYDROCHLORIDE — PHENTERMINE HYDROCHLORIDE (PHENTERMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V037000·2016-01-26

    Altec Recalls 2015 Effer Knuckle Boom Cranes Due to Pedestal Cracks

    Altec Industries is recalling 2015 Effer 440 and 470 Knuckle Boom Cranes because pedestal welds may crack, potentially causing the crane to fall and injure people.

    Product
    EFFER — EFFER 440 KNUCKLE BOOM CRANE, 470 KNUCKLE BOOM CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V038000·2016-01-26

    New Flyer and NABI Buses Recalled for Seat Belt Anchor Defect

    New Flyer is recalling specific 2009-2015 New Flyer and NABI buses because missing welds on seat brackets could allow seat belts to separate during a crash.

    Product
    NABI — NABI, NEW FLYER 40LFW, MD30, XN60, XN35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V039000·2016-01-26

    ShowHauler Recalls 2007-2011 Motorhomes Due to Unstable Entry Steps

    ShowHauler is recalling 2007-2011 motorhomes, garage coaches, and toter coaches because electric entry steps may become unstable, increasing injury risk.

    Product
    SHOWHAULER — SHOWHAULER MOTORHOME, GARAGE COACH, TOTER COACH
    Category
    Vehicle
    Distribution
    Distributed nationwide