The Recall Desk

State

South Carolina product recalls

20,371 recalls have nationwide distribution and so reach South Carolina. 0 additional recalls listed South Carolina specifically in their distribution scope.

About recalls in South Carolina

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect South Carolina consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15301–15325 of 20371

  • HighFDA (Devices)·Z-0095-2023·2022-10-26

    BD Vacutainer Blood Alcohol Testing Tubes Recalled for Analytical Interference

    BD Vacutainer blood collection tubes are recalled due to isobutylene contamination that may cause false positive results in blood alcohol testing.

    Product
    BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0113-2023·2022-10-26

    Reusable Oral Syringe Recalled for Unapproved Plunger Material

    Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.

    Product
    Medicina Reusable Oral syringe 5ml Code: OTH05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0093-2023·2022-10-26

    Siemens N Antiserum to Human IgG Recall for High-Dose Performance Failure

    Siemens Healthcare Diagnostics recalls N Antiserum to Human IgG reagent for laboratory analyzers because it does not meet expected High-Dose Hook Effect performance specifications for IgG measurements in certain sample types.

    Product
    N Antiserum to Human IgG, 2mL Variant for BN II System and BN ProSpec System-IVD Siemens Material Number (SMN): 10446297
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0108-2023·2022-10-26

    Medicina ENFit Enteral Syringes Recalled for Incorrect Plunger Material

    Medicina Uk Ltd is recalling Medicina ENFit 5ml Reusable Enteral Syringes because the plunger component was manufactured with polyethylene instead of the specified polypropylene material.

    Product
    Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2023·2022-10-26

    Rifampin Capsules recalled due to excess nitrosamine impurity

    Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.

    Product
    Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0103-2023·2022-10-26

    Optima Coil System Pouch Labels Do Not Match Carton Labels

    BALT USA is recalling Optima Coil System models OPTI0208CSS10 and OPTI0308CSS10 due to a labeling discrepancy where pouch labels do not match carton labels. These endovascular devices require verification before use.

    Product
    Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0014-2023·2022-10-26

    OTC Sinus Pressure and Pain Cough Product Mislabeled as Decongestant-Free

    Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.

    Product
    SINUS PRESSURE, PAIN AND COUGH — SINUS PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2023·2022-10-26

    FDA Recalls Flunisolide Nasal Solution Due to Out-of-Specification Impurities

    Ingenus Pharmaceuticals is recalling Flunisolide Nasal Solution nationwide because the product contains impurities that exceed acceptable limits. The recall affects two lots distributed across the United States.

    Product
    FLUNISOLIDE — FLUNISOLIDE (FLUNISOLIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·23022·2022-10-25

    Pine-Sol Multi-Surface and All-Purpose Cleaners Recalled for Bacterial Contamination

    Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.

    Product
    Pine-Sol® Scented Multi-Surface Cleaners in Lavender Clean®, Sparkling Wave®, and Lemon Fresh scents, CloroxPro® Pine-Sol® All Purpose Cleaners, in Lavender Clean®, Sparkling Wave®, Lemon Fresh, and Orange Energy® scents, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23021·2022-10-20

    AQUALUNG Apeks Exotec SCUBA Buoyancy Compensators Recalled for Drowning Hazard

    AQUALUNG is recalling Apeks Exotec SCUBA diving buoyancy compensator devices because the dump valve knob can get stuck when inflated, preventing the device from fully inflating and creating a drowning hazard. Approximately 330 units sold nationwide from August 2021 through June 2022 are affected.

    Product
    Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23019·2022-10-20

    Gel Blaster SURGE 1.0 toy guns recalled due to fire hazard

    Gel Blaster is recalling about 62,700 SURGE Model 1.0 toy guns because the lithium-ion battery pack can overheat and ignite. Thirty reports of smoking or fire have been received with no injuries reported.

    Product
    Gel Blaster SURGE 1.0 toy guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23020·2022-10-20

    Birds Choice Acrylic Bird Baths Recalled for Fire Hazard

    Backyard Nature Products is recalling Birds Choice acrylic bird baths because sunlight concentrated through the acrylic can overheat nearby wooden surfaces like siding or decking, creating a fire hazard. Two reports of overheating, smoking, fire, and scorching have been received; no injuries reported.

    Product
    Birds Choice Hanging and Pole-Mounted Acrylic Bird Baths
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23018·2022-10-20

    Mittal International Baby Blankets Recalled for Choking and Strangulation Hazard

    TJX is recalling about 108,000 Mittal International baby blankets sold nationwide from September 2021 through July 2022 because loose threads can detach and pose choking, entrapment, and strangulation hazards to infants.

    Product
    Mittal International Baby Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0017-2023·2022-10-19

    Hobbs Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling transbronchial aspiration needles with incorrect expiration dates on labels. The 18 affected units were distributed in the US, Canada, Austria, Belgium, Finland, and Norway from March 2018 to September 2020.

    Product
    Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kits recalled for incorrect expiration dates

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits due to mislabeled expiration dates that may extend shelf life. Affected devices with lot numbers ending in R were distributed in the US and internationally from 2018-2020.

    Product
    Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0046-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit recalled for incorrect expiration date labeling

    Hobbs Medical recalls the Freeman Pancreatic Flexi-Stent Kit due to incorrect expiration dates on product labels that extend shelf life. Affected devices were distributed to the US and international markets from March 2018 through September 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The incorrect dates extend the shelf life, potentially allowing use beyond the actual safe expiration.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6562
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0026-2023·2022-10-19

    Medical device retrieval basket labels show incorrect expiration dates

    Hobbs Medical recalls the Helical Retrieval Basket due to labels displaying incorrect expiration dates that extend the device's shelf life. Affected units distributed worldwide from March 2018 to September 2020 may be used beyond their validated lifespan.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4806
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0012-2023·2022-10-19

    Hobbs Medical Flex-Ez Guide Wire With Incorrect Expiration Date

    Hobbs Medical Flex-Ez Guide Wire devices were labeled with an incorrect expiration date that extends shelf life beyond the intended duration. Affected devices were distributed in the US and internationally from March 2018 to September 2020.

    Product
    Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0042-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kit Label Bears Incorrect Expiration Date

    Hobbs Medical is recalling Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual product expiration, potentially resulting in use of expired devices.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2023·2022-10-19

    Olympus VC-10 Vacuum Curettage System Recalled for Incompatible Accessories

    Olympus recalls the VC-10 Vacuum Curettage System due to serious injury risk from incompatible collection canisters. The FDA warns users against using accessories not listed in the device's instructions.

    Product
    Berkeley VC-10 Vacuum Curettage System, Model No. VC-10. For transcervical aspiration of the uterine cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0034-2023·2022-10-19

    Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Date Labeling

    Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.

    Product
    Hobbs Medical Grasping Forceps Catalog Number:5004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0056-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Medical Device Recalled for Mislabeled Expiration Date

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates that extend shelf life, affecting devices distributed in the US and five other countries from 2018 to 2020.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6534
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0010-2023·2022-10-19

    Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.

    Product
    Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
    Category
    Medical Device
    Distribution
    Distributed nationwide