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.

56526–56550 of 80986

  • ModerateFDA (Devices)·Z-0315-2016·2015-11-25

    Ameditech Recalls ProScreen Drug Panel Tests Due to Reduced Reactivity

    Ameditech is recalling ProScreen drug panel tests because they have shown reduced reactivity. The recall covers 31,530 units distributed in the US and Australia.

    Product
    ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-10MMO-300, PSCup-10M, PSCupA-10MO, PSCUp-10AB; ProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM; ProScreen 10 Panel Dip Card, Item No. PSD-10MMO-300, PSD-10MOX…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0304-2016·2015-11-25

    Ameditech Recalls CLIA RDTC 12-Panel Drug Abuse Tests for Reduced Reactivity

    Ameditech is recalling 7,482 units of CLIA RDTC 12-Panel Cup drug abuse tests because they have shown reduced reactivity. The products were distributed in the US and Australia.

    Product
    CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12 These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0317-2016·2015-11-25

    Ameditech Recalls Thermo Fisher 6 Drug Cassettes Due to Reduced Reactivity

    Ameditech is recalling Thermo Fisher 6 Drug Cassettes because they have shown reduced reactivity. The recall affects 220 units distributed in the US and Australia.

    Product
    THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0283-2016·2015-11-25

    Agfa Healthcare Recalls IMPAX CV Software for Incorrect PDF Reports

    Agfa Healthcare is recalling IMPAX CV software versions 7.8.x and 12.x because the Demographics Manager feature may generate incorrect PDF reports after physician signature.

    Product
    IMPAX, PACS, Picture Archive and Communications System, IMPAX CV 7.8.x and IMPAX CV 12.x. Corrects certain demographic information (Patient Name, Patient Medical Record Number and/or Accession Number in previously signed reports that have since changed.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0309-2016·2015-11-25

    Ameditech Recalls DrugSmart Dip Drug Abuse Tests Due to Reduced Reactivity

    Ameditech is recalling 160 units of DrugSmart Dip drug abuse tests because they have shown reduced reactivity. The affected products were distributed in the US and Australia.

    Product
    DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D; DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0187-2016·2015-11-25

    Herr's Potato Chips Recalled for Incorrect Gluten-Free Labeling

    Herr's Foods is recalling Sour Cream & Onion Potato Chips because packaging incorrectly states the product is gluten-free, despite containing wheat.

    Product
    Herr's Sour Cream & Onion Flavored Potato Chips
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-0308-2016·2015-11-25

    Ameditech Recalls DrugSmart Drug Abuse Test Cups Due to Reduced Reactivity

    Ameditech is recalling specific DrugSmart drug abuse test cups because they have shown reduced reactivity. The affected units were distributed in the US and Australia.

    Product
    DrugSmart 11 Test Cup, Item No. 61127D; DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D; DrugSmart 9 Test Cup (BUP), Item No. 60960D; DrugSmart Cup 10, Item No. 61093D-3C These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0314-2016·2015-11-25

    Ameditech Recalls Premier Clia Waived 12 Panel Tilt Cup Drug Tests

    Ameditech is recalling Premier Clia Waived 12 Panel Tilt Cup drug tests because they have shown reduced reactivity.

    Product
    Premier Clia Waived 12 panel Tilt Cup, Item No. C12APC These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0316-2016·2015-11-25

    Ameditech Recalls 6 Panel Drug Detection Cups Due to Reduced Reactivity

    Ameditech is recalling 2,240 units of 6 Panel Cup Body and Lid drug tests because they have shown reduced reactivity.

    Product
    The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0307-2016·2015-11-25

    Ameditech Recalls DrugSmart 10 Test Cups Due to Reduced Reactivity

    Ameditech is recalling DrugSmart 10 Test Cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.

    Product
    DrugSmart 10 Test Cup (PCP & MDMA), Item No. 61055D; DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0299-2016·2015-11-25

    Ameditech Recalls 10-Panel Pipette Drug Screen Due to Reduced Reactivity

    Ameditech is recalling 10-Panel Pipette Drug Screen tests because they have shown reduced reactivity. The recall affects 200 units distributed in the US and Australia.

    Product
    10-Panel Pipette Drug Screen, Item No. PSP-10M These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0305-2016·2015-11-25

    Ameditech Recalls DrugCheck Pipette 10 Drug Tests Due to Reduced Reactivity

    Ameditech is recalling 70 units of DrugCheck Pipette 10 Drug Tests because they have shown reduced reactivity. The affected tests were distributed in the US and Australia.

    Product
    DrugCheck Pipette 10 Drug Test, Item No. 41025 DC These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0235-2016·2015-11-25

    Mylan Recalls Meclizine Hydrochloride Tablets Due to Impurity Failures

    Mylan Institutional is recalling 4,609 packages of Meclizine Hydrochloride 25 mg tablets because they failed impurity specifications.

    Product
    Meclizine Hydrochloride Tablets, USP, 25 mg Tablets, Packaged in 10 x 10 Tablet Blister Pack Packages, Rx Only. Manufactured by: Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977. Mylan. NDC: 51079-090-20.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0302-2016·2015-11-25

    Ameditech Recalls 12-Panel Dip Drug Screens Due to Reduced Reactivity

    Ameditech is recalling 12-Panel Dip Drug Screens with adulterant because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.

    Product
    12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0295-2016·2015-11-25

    Akorn Recalls Hydrocortisone Otic Solution Due to Missing Safety Seal

    Akorn, Inc. is recalling 13,896 bottles of Hydrocortisone and Acetic Acid Otic Solution because the bottles are missing the safety seal around the neck.

    Product
    Hydrocortisone and Acetic Acid Otic Solution, USP, containing hydrocortisone (1%) and acetic acid (2%), 10 mL bottles, Rx Only, Hi-Tech Pharmacal, Amityville, NY 11701, Made in USA, NDC # 50383-901-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0231-2016·2015-11-25

    Akorn Recalls RIFAMPIN FOR INJECTION Due to Impurity Specifications

    Akorn, Inc. is recalling 6,861 vials of RIFAMPIN FOR INJECTION USP, 600 mg because a known impurity failed to meet specifications.

    Product
    RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0233-2016·2015-11-25

    Par Pharmaceutical Recalls Meclizine Hydrochloride Tablets Due to Impurities

    Par Pharmaceutical is recalling specific lots of Meclizine Hydrochloride 12.5 mg tablets because they failed impurity specifications.

    Product
    Meclizine Hydrochloride Tablets, USP, 12.5 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-034-01) and b) 1000 Ct Bottles (NDC: 49884-034-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0291-2016·2015-11-25

    Baxter HomeChoice APD Systems Recalled for Loud Operating Sounds

    Baxter is recalling HomeChoice and HomeChoice Pro APD systems due to loud operating sounds. The devices function correctly, but the noise is unacceptable to users.

    Product
    Baxter HomeChoice and HomeChoice Pro APD systems, designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V796000·2015-11-24

    Mercedes-Benz Recalls 2015 S550E Hybrid Vehicles Due to Charger Defect

    Mercedes-Benz is recalling 2015 S550E Hybrid vehicles because a defective onboard charger may cause the car to unexpectedly shift to park, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S550E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V792000·2015-11-24

    Mercedes-Benz Recalls 2014 E350 Sedans for Fuel Line Fire Risk

    Mercedes-Benz is recalling 809 model year 2014 E350 sedans because a fuel feed line defect may cause a leak or disconnection, increasing the risk of fire or a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16045·2015-11-24

    SalesOne Recalls Light Up Ear Plug Jewelry Due to Burn Hazard

    SalesOne is recalling light-up ear plug jewelry sold at Spencer Gifts because battery acid can leak and cause burns. Consumers should stop wearing the product and contact SalesOne for a refund or replacement.

    Product
    Light up ear plug jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V791000·2015-11-24

    Wabash National Van Trailers Recalled for Brake Caliper Bolt Defect

    Wabash is recalling 2013-2015 Van Trailers because brake caliper bolts may not be tightened, risking caliper detachment and reduced braking.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V794000·2015-11-24

    Subaru Recalls 2016 Legacy and Outback for Drive Shaft Separation Risk

    Subaru is recalling 2016 Legacy and Outback vehicles because improperly tightened nuts may allow the drive shaft to separate, potentially causing a fuel leak and fire.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V790000·2015-11-24

    VT Hackney Recalls 2015 Kidron Refrigerated Trailers Due to Brake Defect

    VT Hackney is recalling certain 2015 Kidron Refrigerated Trailers because improperly tightened caliper bolts may allow the brake caliper to detach, reducing braking performance.

    Product
    KIDRON — KIDRON REFRIGERATED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V789000·2015-11-24

    Ford Recalls 2016 F-650 Trucks Due to Incorrect Steering Column

    Ford is recalling 2016 F-650 trucks built between July 29 and September 3, 2015, because an incorrect steering column may cause the park pawl to fracture, allowing the vehicle to move unexpectedly.

    Product
    FORD — FORD F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide