State

South Carolina product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53251–53275 of 80980

ModerateFDA (Devices)·Z-2084-2016·2016-07-06
Integra LifeSciences Recalls METASURG Capture Screw System K-wires
Integra LifeSciences is recalling 182 K-wires used in the METASURG Capture Screw System because they do not meet material, surface, and dimensional specifications.
Product
K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in conjunction with the 2.0 mm cannulated screws for the METASURG Capture Screw System. The K-wire is used by the physician to insert into the bone and to act as a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2116-2016·2016-07-06
Philips Brilliance 64 CT Scanner Recall for Image Artifacts
Philips is recalling 94 Brilliance 64 CT scanners due to intermittent swirl-like ring artifacts on images, which may require patient rescans.
Product
Brilliance 64, Computed Tomography X-ray system Product Usage: The Brilliance CT 64 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1052-2016·2016-07-06
Lupin Recalls Lisinopril and Hydrochlorothiazide Tablets Due to CGMP Deviations
Lupin Pharmaceuticals is recalling specific lots of Lisinopril and Hydrochlorothiazide tablets because they were manufactured using active ingredients that failed specifications.
Product
LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1053-2016·2016-07-06
Aloe Source Recalls Topical Analgesic Products Due to Manufacturing Deviations
The Aloe Source is voluntarily recalling specific lots of aloe SPORT liniment and eucalyptus cream due to CGMP deviations.
Product
aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube, ALOE VERA Liniment Topical Analgesic 8 fl oz. bottle, Manufactured by Coats International, Inc., the ALOE SOURCE SPORT Sport Thermogenic Eucalyptus Cream 1 fl oz. plastic bottle, Dallas, TX 75243, NDC 58826-704-08, UPC…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1061-2016·2016-07-06
Aidarex Recalls Ciprofloxacin Ophthalmic Solution Due to Unknown Impurity
Aidarex Pharmaceuticals is recalling 599 bottles of Ciprofloxacin Ophthalmic Solution because testing revealed out-of-specification results for an unknown impurity.
Product
Ciprofloxacin OPTH 0.3% SOL, generic for: Ciloxan, Rx Only, 2.5 mL Bottle, Repackaged by: Aidarex Pharmaceuticals, MFG: Hi-Tech Pharmacal Co., Inc., Amityville, NY, 11701, NDC a) 33261-0910-01, b) 33261-0614-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1057-2016·2016-07-06
KVK-Tech Recalls Benzphetamine Hydrochloride Tablets Due to Cosmetic Scuffing
KVK-Tech, Inc. is recalling specific lots of Benzphetamine Hydrochloride Tablets due to cosmetic scuffing marks on the tablets.
Product
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1059-2016·2016-07-06
Valeant Recalls Secobarbital Sodium Capsules Due to Missing Anaphylaxis Warning
Valeant Pharmaceuticals is recalling 958 bottles of SECONAL SODIUM capsules because the package insert is missing a warning regarding anaphylaxis.
Product
SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2051-2016·2016-07-06
Cardiovascular Systems Recalls ViperWire Advance Peripheral Guide Wire Due to Missing Date
Cardiovascular Systems Inc is recalling ViperWire Advance Peripheral Guide Wire because the pouch label was missing the use-by date.
Product
ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1058-2016·2016-07-06
CVS Acid Controller Tablets Recalled for Impurity Specification Failure
Dr. Reddy's is recalling CVS pharmacy Acid Controller tablets because stability testing revealed an out-of-specification impurity.
Product
CVS pharmacy Original Strength Acid Controller tablets, 10 mg, 30-count bottle, OTC, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 150049523
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V507000·2016-07-05
GM Recalls 2009-2010 Chevrolet Impala for Passenger Air Bag Wiring Defect
General Motors is recalling 2009-2010 Chevrolet Impalas because the front passenger seat frame may damage sensor wires, potentially disabling air bags or seat belt pretensioners in a crash.
Product
CHEVROLET — CHEVROLET IMPALA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V503000·2016-07-05
Utility Recalls 2014-2016 Trailers Due to Spring Brake Valve Defect
Utility Trailer Manufacturing Company is recalling 2014-2016 flatbed, refrigerated, and dry van trailers because improperly machined spring brake valves may delay braking, increasing crash risk.
Product
UTILITY — UTILITY FLATBED TRAILERS, REFRIGERATED TRAILERS, DRY VAN TRAILERS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V505000·2016-07-05
VT Hackney Recalls Kidron and Hackney Trailers Due to Brake Defect
VT Hackney is recalling 2014-2016 Kidron and Hackney trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Product
KIDRON — KIDRON, HACKNEY REFRIGERATED TRAILER, BEVERAGE TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V506000·2016-07-05
East Manufacturing Recalls 2014-2016 Trailers Due to Brake Valve Defect
East Manufacturing is recalling 290 model year 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Product
EAST — EAST FLATBED, FRAME DUMP, FLATBED TIPPER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V502000·2016-07-05
GM Recalls Vehicles for Ignition Key Removal and Rollaway Risk
General Motors is recalling specific Buick, Chevrolet, and GMC vehicles because the ignition key may be removed without the transmission in Park, creating a rollaway hazard.
Product
CHEVROLET — CHEVROLET, BUICK, GMC EQUINOX, REGAL, CRUZE, TERRAIN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V500000·2016-07-05
Forest River Recalls Orion, Rockport, and Rev Vehicles for Brake Light Software Error
Forest River is recalling certain 2014-2017 Orion, Rockport, and Rev vehicles because a software error may prevent trailer brake lights from illuminating, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER ROCKPORT, ORION, REV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16C006000·2016-07-05
Combi Coccoro Convertible Child Restraints Recalled for Crash Injury Risk
Combi is recalling Coccoro Convertible Child Restraints because excessive force may be transmitted to the occupant in a crash if the seat is forward-facing and secured only with a lap belt.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V501000·2016-07-05
Newmar Recalls Motorhomes Due to Exhaust Tube Fire Risk
Newmar is recalling specific model year 1998-2015 motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase the risk of a fire.
Product
NEWMAR — NEWMAR KOUNTRY STAR, VENTANA, DUTCH STAR, ALL STAR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V504000·2016-07-05
Jerr-Dan Recalls 2014-2016 HDR 1000 Wrecker Trucks Due to Control Defect
Jerr-Dan is recalling 24 model year 2014-2016 HDR 1000 wrecker trucks because vehicle-mounted controls may remain engaged, causing unintended equipment movement and injury risk.
Product
JERR-DAN — JERR-DAN HDR 1000
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V496000·2016-07-01
Wilson Trailer Company Recalls 2015 CD-1080 and DWH-550 Trailers
Wilson Trailer Company is recalling 2015 CD-1080 and DWH-550 trailers due to improperly machined spring brake valves that may delay braking, increasing the risk of the trailer rolling away.
Product
WILSON — WILSON CD-1080, DWH-550
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V499000·2016-07-01
Mazda Recalls B-Series Trucks Due to Air Bag Inflator Rupture Risk
Mazda is recalling 2007-2009 B-Series trucks in specific regions because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Product
MAZDA — MAZDA B-SERIES TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V495000·2016-07-01
FCA Recalls 2016 Ram Trucks Due to Transfer Case Shaft Fracture Risk
FCA is recalling 2016 Ram 3500, 4500, and 5500 trucks because a misshapen transfer case shaft may fracture, potentially causing loss of motive power or rollaway.
Product
RAM — RAM 5500, 3500, 4500
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·054-2016·2016-07-01
GHSE Recalls Chicken Salads Due To Undeclared Wheat Allergen
GHSE, LLC is recalling approximately 5,682 pounds of ready-to-eat chicken salads because the packaging labels failed to declare wheat, a known allergen.
Product
GHSE, LLC — GHSE, LLC Recalls Chicken Products Due To Misbranding And Undeclared Allergen
Category
Food
Distribution
7 states
HighNHTSA·16V497000·2016-07-01
Ameritrans Shuttle Buses Recalled for Incorrect Tire and Loading Placards
Ameritrans is recalling 2012-2016 shuttle buses because incorrect tire and loading placards may confuse operators and lead to vehicle overloading.
Product
AMERITRANS — AMERITRANS E350, 5500, E450, F550
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V494000·2016-07-01
Fontaine Recalls 2015-2017 Revolution Trailers Due to Brake Valve Defect
Fontaine is recalling 2015-2017 Revolution trailers because improperly machined brake valves may delay spring brake application, increasing the risk of the trailer rolling away.
Product
FONTAINE — FONTAINE REVOLUTION
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16207·2016-07-01
Winco Recalls Black Cat Cone Fountain Fireworks Due to Fire Hazard
Winco Fireworks is recalling Black Cat Cone Fountain Fireworks because they may burst and spread sparks outward, posing fire and burn risks.
Product
Cone Fountain Fireworks
Category
Consumer Product
Distribution
Distributed nationwide