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.

57176–57200 of 80986

SevereFDA (Drugs)·D-1833-2015·2015-10-07
Medistat RX Recalls Sterile Products Due to Sterility Assurance Concerns
Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.
Product
All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-3248-2015·2015-10-07
General Mills Recalls Cascadian Farm Organic Cut Green Beans for Listeria
General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.
Product
Cascadian Farm Organic Cut Green Beans, Net Wt. 10 oz (284g) Keep Frozen.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0003-2016·2015-10-07
Biosense Webster Recalls SOUNDSTAR eco Diagnostic Ultrasound Catheters
Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.
Product
SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2824-2015·2015-10-07
Medtronic Navigated Solera Screwdrivers Recalled for Potential Tip Deformation
Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.
Product
P/N: 9734856, SCREWDRIVER, 9734856, SOLERA STD MAST; P/N: 9734857, SCREWDRIVER, 9734857, SOLERA RDN MAST; P/N: 9734279, SCREWDRIVER 9734279 SOLERA STANDARD; and P/N: 9734373, SCREWDRIVER 9734373 SOLERA REDUCTION. The Medtronic Navigated Solera Screwdrivers are reusable devices…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0002-2016·2015-10-07
Biosense Webster Recalls Carto 3 EP Navigation System Due to Image Loss
Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.
Product
Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V630000·2015-10-07
Volvo Recalls 2015-2016 Trucks for Headlight Intensity Defect
Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.
Product
VOLVO — VOLVO VAH, VHD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-3257-2015·2015-10-07
KAL Amino Acid Complex Recalled for Undeclared Milk Allergen
Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.
Product
KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
Category
Food
Distribution
Distributed nationwide
HighCPSC·16701·2015-10-07
BRP Recalls Youth Can-Am ATVs Due to Fuel Filter Fire Hazard
BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.
Product
Youth Model Can-Am all-terrain vehicles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2823-2015·2015-10-07
Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk
Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.
Product
P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2822-2015·2015-10-07
MicroAire LipoTower Recalled for Potential Electrical Shock Hazard
MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.
Product
ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2826-2015·2015-10-07
Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect
Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.
Product
Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2821-2015·2015-10-07
MicroAire LipoTower Recall Due to Electrical Shock Risk
MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.
Product
ASP-1020 LipoTower with Aspiration Pump. Medical use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2820-2015·2015-10-07
Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling
Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.
Product
Zimmer Guide Wires for orthopedic procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0004-2016·2015-10-07
Lifeline Systems Recalls Philips GoSafe Mobile Help Button Due to Battery Issues
Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.
Product
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0005-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2819-2015·2015-10-07
Sterilmed Recalls Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling
Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.
Product
Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0001-2016·2015-10-07
Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2818-2015·2015-10-07
Olympus Recalls Gastrovideoscope Due to Insufficient Cleaning Accessory Information
Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.
Product
EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·F-3264-2015·2015-10-07
Dixie Crystals Sugar Recalled for Foreign Matter Detection
Savannah-Imperial LP is recalling specific lots of Dixie Crystals sugar due to the detection of blue fiber in the product.
Product
Dixie Crystals, Sugar EFG, Net Weight 50 lbs and 2000 lbs., Imperial Sugar Company, Savannah, GA.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3259-2015·2015-10-07
Imperial Sugar Recalls Granulated Sugar Due to Foreign Matter
Savannah-Imperial LP is recalling 50-pound bags of Imperial Sugar granulated sugar because blue fiber was detected in the product.
Product
Imperial Sugar, Pure Granulated Sugar, Net wt. 50 lbs (22.6 kg), Distributed by Imperial-Savannah LP, Sugar Land, Texas 77478.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3261-2015·2015-10-07
Monarch Granulated Sugar Recalled for Foreign Matter Detection
Savannah-Imperial LP is recalling Monarch Granulated Sugar due to the detection of blue fiber in the product.
Product
Monarch, Granulated Sugar, Net Wt. 25 lbs and 50 lbs (22.88 kg), Distributed by US Foods, Inc., Rosemont, IL.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3260-2015·2015-10-07
West Creek Granulated Sugar Recalled for Foreign Matter
Savannah-Imperial LP is recalling West Creek Extra Fine Granulated Sugar because blue fiber was detected in the product.
Product
West Creek, Extra Fine Granulated Sugar, Net Wt. 25 lbs (11.3 kg), Distributed by Performance Food Group, Richmond, VA 23238.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3265-2015·2015-10-07
Imperial Sugar Recalls 2000 lb Bags Due to Foreign Matter
Savannah-Imperial LP is recalling 2000 lb bags of Imperial GMI Non GMO Linerless Sugar EFG because blue fiber was detected in the product.
Product
Imperial GMI, Non GMO Linerless Sugar EFG, Net Weight 2000 lbs., Imperial Sugar Company, Savannah, GA.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3262-2015·2015-10-07
Savannah-Imperial Recalls Clear Value Sugar Due to Foreign Matter
Savannah-Imperial LP is recalling Clear Value Sugar because blue fiber was detected in the product.
Product
Clear Value Sugar, granulated, Net Wt. 4 lbs (1.81 kg), Distributed by Topco Associates LLC, 7711 Gross Point Road, Skokie, IL 60077.
Category
Food
Distribution
17 states
LowFDA (Food)·F-3266-2015·2015-10-07
Laura Lynn Pure Cane Sugar Recalled for Foreign Matter
Savannah-Imperial LP is recalling Laura Lynn Pure Cane Sugar because blue fiber was detected in the product.
Product
Laura Lynn, Pure Cane Sugar, Net Wt. 25 lbs (11.34 kg), Distributed by Ingles Markets, Inc., Asheville, NC 26816.
Category
Food
Distribution
17 states