The Recall Desk

State

South Carolina product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39526–39550 of 80893

  • ModerateFDA (Drugs)·D-1208-2019·2018-12-05

    Akorn Recalls Clindamycin Phosphate Topical Solution Due to Impurity Failures

    Akorn, Inc. is recalling 58,393 jars of Clindamycin Phosphate Topical Solution USP, 1% because the product failed impurity and degradation specifications.

    Product
    Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0509-2019·2018-12-05

    Tosoh AIA-900 Analyzer Recalled for Potential Drive Motor Failure

    Tosoh Bioscience is recalling 247 AIA-900 Automated Immunoassay Analyzers due to a potential drive motor defect that may cause the device to stop functioning and delay patient test results.

    Product
    AIA-900 Automated Immunoassay Analyzer, product code 022930 /022930R Product Usage: The AIA-900 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0499-2019·2018-12-05

    Siemens Dimension Vista Lactate Dehydrogenase Reagent Cartridge Recall

    Siemens is recalling Dimension Vista Lactate Dehydrogenase reagent cartridges because they may produce falsely elevated results if used after Lactic Acid assays.

    Product
    Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge, an in vitro diagnostic test for the quantitative measurement of lactate dehydrogenase in human serum and plasma on the Dimension Vista¿ System.Cat. No. K2054, Mat. No. 10464323
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0516-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to confirmed foreign substance contamination.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg 16.5 GAL Catalog Number: OFD2201-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V859000·2018-12-04

    Newmar Recalls 2018-2019 Motorhomes Due to Loose Brake Caliper Bolts

    Newmar is recalling 2018-2019 Essex, Ventana, and London Aire motorhomes because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·085-2018 EXP·2018-12-04

    JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport

    JBS Tolleson is recalling approximately 12.1 million pounds of raw beef products, including ground beef, due to possible Salmonella Newport contamination.

    Product
    JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·19720·2018-12-04

    Foremost Recalls Glass Shower Doors and Panels Due to Hinge Failure

    Foremost is recalling about 700 glass shower doors and panels because pivot hinges can fail, causing the glass to separate from the frame and fall or shatter.

    Product
    Glass shower doors and panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V857000·2018-12-03

    Gulf Stream Vintage Cruiser Recalled for Insufficient Bearing Grease

    Gulf Stream is recalling 2019 Vintage Cruiser recreational trailers because inner hub bearings may lack sufficient grease, risking overheating and hub failure.

    Product
    GULF STREAM — GULF STREAM VINTAGE CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V858000·2018-12-03

    McNeilus and Oshkosh Trucks Recalled for CNG Valve Defect

    McNeilus is recalling 2016-2018 trucks and Oshkosh S-Series vehicles because a CNG fuel tank valve stem may eject, posing injury and fire risks.

    Product
    OSHKOSH — OSHKOSH, MCNEILUS S-SERIES, XE REAR LOADER, STANDARD MIXER, BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V856000·2018-12-03

    Forest River Recalls 2019 Salem and Wildwood Trailers for Wiring Defect

    Forest River is recalling 2019 Salem and Wildwood recreational trailers because incorrectly wired clearance lights may not work, reducing visibility.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E111000·2018-12-01

    Luxfer Recalls One-Turn Valves Due to Potential Stem Ejection Risk

    Luxfer Canada Ltd. is recalling One-Turn Valves (part number MPVE-250) because the valve stem may forcibly eject if the knob is turned more than one turn, posing injury and fire risks.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V853000·2018-11-30

    Keystone Recalls 2019 Montana Trailers Due to Axle Weld Defects

    Keystone RV Company is recalling 2019 Montana recreational trailers because defective axle welds could cause the wheel assembly to detach, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V852000·2018-11-30

    Heartland Recalls 2019 Fifth-Wheel Trailers for Missing Reflectors

    Heartland is recalling 2019 fifth-wheel trailers because forward reflectors may be missing, reducing visibility and increasing crash risk.

    Product
    HEARTLAND — HEARTLAND MILESTONE, ELK RIDGE, SUNDANCE, PIONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V851000·2018-11-30

    Jayco Recalls 2019 Travel Trailers Due to Insufficient Wheel Bearing Grease

    Jayco is recalling 2019 Jay Flight SLX, Jay Feather, and White Hawk travel trailers because inner wheel hub bearings may lack sufficient grease, risking overheating and hub failure.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK, JAY FLIGHT SLX, JAY FEATHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V850000·2018-11-29

    Mercedes-Benz Recalls Vehicles Due to Steering Rack Locknut Failure Risk

    Mercedes-Benz is recalling specific 2015-2019 models because a steering rack locknut may break, causing the steering to stick and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 350 E, E 300, C 300, CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V849000·2018-11-29

    Mercedes-Benz Recalls 2019 Wagons Due to Spoiler Detachment Risk

    Mercedes-Benz is recalling 2019 E450 and E63S Wagons because the tailgate spoiler may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, AMG E63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V837000·2018-11-29

    Mercedes-Benz Metris Fuel Hose Leak Recall

    Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vehicles because a fuel hose may leak, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0269-2019·2018-11-28

    Sciegen Recalls Irbesartan Tablets Due to NDEA Impurity

    Sciegen Pharmaceuticals is recalling Irbesartan 300mg tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).

    Product
    Westminister Irbesartan Tablets, USP, 300mg, Rx Only,(a) 30-count bottle (NDC 69367-121-01, (b) 90-count bottle (NDC 69367-121-03), Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755. Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854 Made in…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0270-2019·2018-11-28

    Sciegen Pharmaceuticals Recalls Irbesartan Tablets Due to NDEA Impurity

    Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 75 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).

    Product
    GSMS Irbesartan Tablets, USP, 75 mg, 30-count bottle, Rx Only, Manufactured by ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Marketed by: GSMS Incorporated Camarillo, CA 93012 USA, NDC 60429-640-90.
    Category
    Drug
    Distribution
    Distributed nationwide