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.

31776–31800 of 80889

HighFDA (Devices)·Z-2044-2020·2020-05-27
Medline Recalls Silicone Foley Catheters Due to Loose Particulate
Medline Industries is recalling specific lots of silicone Foley catheters because loose silicone particulate was found on the device shaft.
Product
SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml - Product Usage: Medline Silicone Foley catheter is a flexible tubular device that is inserted through the urethra and used to drain urine into a collection device.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20E033000·2020-05-27
Horizon Recalls Tekonsha Prodigy Electronic Brake Control Kits
Horizon Global is recalling certain Tekonsha Prodigy electronic brake control kits because they do not adequately warn drivers that foot pedal trailer braking is unavailable when hazard signals are active.
Product
ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2051-2020·2020-05-27
Cardinal Health Recalls Strep B Carrot Broth Due to Temperature Abuse
Cardinal Health is recalling Strep B Carrot Broth One-Step tubes because they were stored outside approved temperature ranges, which may lead to patient misdiagnosis.
Product
Strep B Carrot Broth One-Step, 16x100mm Tube, 6ml, Item code Z46BX - Product Usage: Intended to detect Group B Streptococcus (GBS) from anovaginal specimen collected from pregnant women. If pregnant woman is positive for GBS colonization, this will indicate a need for treatment…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V308000·2020-05-27
Thor Motor Coach Recalls 2020 Motorhomes Due to Manual Error
Thor Motor Coach is recalling 566 2020 motorhomes because the owner's manual incorrectly describes the automatic parking function, which could lead to vehicle rollaway.
Product
THOR MOTOR COACH — THOR MOTOR COACH, THOR SIESTA, SYNERGY, GEMINI, DELANO
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1282-2020·2020-05-27
West-Ward Recalls Ethacrynic Acid Tablets for Impurity Failures
West-Ward Columbus Inc is recalling Ethacrynic Acid Tablets USP, 25 mg, because the product failed impurity and degradation specifications.
Product
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·20127·2020-05-27
Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels
Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.
Product
Wide Fit Kitten Heel Court Pumps
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2064-2020·2020-05-27
Philips HeartStart MRx Processor Board Replacement Kits Recalled for Damaged Bags
Philips is recalling HeartStart MRx Processor Board PCA Replacement Kits because damaged ESD bags were used for storing components.
Product
HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Product Usage: is intended for use in hospital and prehospital settings by qualified medical personnel trained in the operation of the device and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2045-2020·2020-05-27
Boston Scientific Recalls AMS 700 Reservoirs Due to Labeling Error
Boston Scientific is recalling five AMS 700 100 mL Spherical Reservoirs with InhibiZone because they were incorrectly labeled as a different model.
Product
AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the treatment of chronic, organic, male erectile dysfunction (impotence).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2067-2020·2020-05-27
DFINE Vertebral Hydraulic Assemblies Recalled for Incorrect Expiration Dates
Merit Medical Systems is recalling 228 DFINE Vertebral Hydraulic Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 1402 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological fractures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2073-2020·2020-05-27
Capso Vision Recalls CapsoCam Plus Capsule Endoscopy Systems Due to Labeling Errors
Capso Vision, Inc. is recalling 44 CapsoCam Plus video capsule systems because incorrect serial number labels may lead to patient misdiagnosis.
Product
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2020·2020-05-27
Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates
Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1271-2020·2020-05-27
Mylan Recalls Aloprim Injection Vials Due to Discoloration
Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.
Product
ALOPRIM — ALOPRIM (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1272-2020·2020-05-27
InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure
InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2038-2020·2020-05-27
Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch
Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.
Product
Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V301000·2020-05-26
Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings
Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V302000·2020-05-26
2020-2021 Keystone Cougar travel trailer cooktop fire hazard
Keystone is recalling 2020-2021 Cougar travel trailers because the cooktop may not be properly sealed from the furnace, causing burner flames to invert and increasing fire risk. Dealers will inspect and seal it free of charge.
Product
KEYSTONE — KEYSTONE COUGAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V300000·2020-05-23
AEV TraumaHawk Ambulances Recalled for Rear Brake Line Wear Risk
Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.
Product
AEV — AEV TRAUMAHAWK
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·007-2020-EXP ·2020-05-22
Conagra Recalls Frozen Chicken and Turkey Bowls Due to Rock Contamination
Conagra Brands is recalling approximately 276,872 pounds of frozen Healthy Choice Power Bowls because they may contain small rocks. No illnesses have been reported.
Product
Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·20V298000·2020-05-22
Mercedes-Benz Recalls 2012 C-Class Vehicles for Incorrect Air Bag Replacement
Mercedes-Benz is recalling 2012 C-Class vehicles where an incorrect front passenger air bag may have been installed during a prior recall, potentially reducing crash protection.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300, AMG C63, C250, C350
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V297000·2020-05-22
2020-2021 Forest River Surveyor Travel Trailers Safety Chain Recall
Forest River is recalling 2020-2021 Surveyor travel trailers because the safety chains are insufficient for the trailer's weight rating and may break if the trailer becomes unhitched, risking complete detachment.
Product
FOREST RIVER — FOREST RIVER SURVEYOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V299000·2020-05-22
Triple E Recalls 2020 Unity Travel Trailers Due to Latch Defect
Triple E is recalling 2020 Unity travel trailers because a latch may lock, blocking access to the propane shutoff valve and increasing fire risk.
Product
TRIPLE E — TRIPLE E UNITY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V296000·2020-05-22
KZRV Recalls 2018 Escape Trailers Due to Incorrect Tire Labels
KZRV is recalling 2018 Escape recreational trailers because incorrect tire labels may cause overinflation, increasing crash risk.
Product
KZRV — KZRV ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V294000·2020-05-21
Dennis Eagle Elite Garbage Trucks Recalled for Braking System Defect
Dennis Eagle is recalling 2017-2018 Elite garbage trucks because the anti-lock braking system may activate on the wrong side, increasing stopping distance.
Product
DENNIS EAGLE — DENNIS EAGLE ELITE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V295000·2020-05-21
2021 Chevrolet Trailblazer lacks tire size and pressure label information
General Motors is recalling certain 2021 Chevrolet Trailblazer vehicles with optional sport terrain tires because their certification labels do not show tire size and cold tire pressure information required by federal safety standards.
Product
CHEVROLET — CHEVROLET TRAILBLAZER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20746·2020-05-21
Viva Doria Recalls Wintergreen Essential Oil Due to Packaging Defect
Viva Doria is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Product
Viva Doria Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide