State

South Carolina product recalls

73,509 recalls have nationwide distribution and so reach South Carolina. 7,146 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,146
Critical: 1,278
Severe: 2,166
Most recent: 2026-10-14

Of the 7,146 recalls naming South Carolina we have scored against our rubric, 1,278 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,166 (30%) are Severe.

Which agencies issued them

These figures cover only the 7,146 recalls whose distribution notice names South Carolina specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24001–24025 of 80655

ModerateFDA (Drugs)·D-0492-2022·2022-02-09
Drug Recall: PAINAID Tablets for Manufacturing Deviations
Ultra Seal Corporation is recalling approximately 2.3 million packets of PAINAID pain relief tablets nationwide due to cGMP (current Good Manufacturing Practice) deviations in manufacturing processes.
Product
PAINAID (acetaminophen 110 mg, aspirin 162mg, caffeine 32.4 mg, salicylamide 152mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0500-2022·2022-02-09
Magnacal Calcium Carbonate Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is recalling MAGNACAL calcium carbonate 420 mg tablets (Lot #AK9768, expiration 08/2022) nationwide due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall was initiated on January 24, 2022.
Product
MAGNACAL (calcium carbonate 420 mg), 2 tablet packets, Manufactured for: Afassco Inc. Minden, NV 89423
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0522-2022·2022-02-09
Prescription Drug Recall: Mimvey Mislabeling by Teva Pharmaceuticals
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling. The recall affects 6,430 cartons distributed throughout the USA.
Product
MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0521-2022·2022-02-09
Mimvey Estradiol/Norethindrone Prescription Drug Mislabeling Recall
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling on certain cartons. The recall affects 218,174 cartons distributed in the United States.
Product
MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V066000·2022-02-08
Mercedes-Benz Metris Recall for Brake Fluid Reservoir Mounting Defect
Daimler Vans USA is recalling 2016-2021 Mercedes-Benz Metris vehicles because the brake fluid reservoir may detach, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V068000·2022-02-08
Tiffin motorhomes have improperly secured buss bars increasing fire risk
Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.
Product
TIFFIN — TIFFIN ALLEGRO, ALLEGRO BREEZE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V067000·2022-02-08
Holiday House Travel Trailers Propane Regulator Failure Risk
Holiday House is recalling certain 2019–2021 travel trailers equipped with defective Winntec propane regulators that may fail and increase propane pressure, raising fire risk in gas appliances.
Product
HOLIDAY HOUSE — HOLIDAY HOUSE 24TB, 27RQ, 18RB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V065000·2022-02-07
Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines
Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.
Product
ROADTREK — ROADTREK ZION SRT, ZION SLUMBER, ZION, PLAY SLUMBER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V064000·2022-02-07
Audi Recalls 2022 Q3 Vehicles for Rearview Camera Software Error
Audi is recalling 2022 Q3 vehicles because a software error may prevent the rearview camera from displaying an image when reversing, increasing crash risk.
Product
AUDI — AUDI Q3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V063000·2022-02-04
Tesla Model Y Boombox Feature May Obscure Pedestrian Warning System
Tesla is recalling certain 2020-2022 Model Y vehicles because the Boombox feature can obscure the Pedestrian Warning System sounds, creating a collision risk. Tesla will disable the Boombox in Drive, Neutral, and Reverse modes via software update.
Product
TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V062000·2022-02-04
Triumph Recalls 2022 Trident 660 Motorcycles Due to Side Stand Defect
Triumph is recalling 2022 Trident 660 motorcycles because the side stand may bend under weight, causing the bike to become unstable while parked.
Product
TRIUMPH — TRIUMPH TRIDENT 660
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V056000·2022-02-03
Hyundai Recalls Vehicles Due to ABS Module Fire Risk
Hyundai is recalling specific 2014-2019 models because a faulty ABS module could cause an electrical short and engine compartment fire.
Product
HYUNDAI — HYUNDAI TUCSON, SANTA FE, SANTA FE SPORT, SANTA FE XL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V061000·2022-02-03
Honda Recalls 2021 CBR1000RR-R Fireblade SP Motorcycles for Fire Risk
Honda is recalling 2021 CBR1000RR-R Fireblade SP motorcycles because an overheating exhaust pipe could melt the oil cooler pipe, causing a leak that increases the risk of fire or crash.
Product
HONDA — HONDA CBR1000RR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V060000·2022-02-03
Altec Recalls 2021 Aerial Devices Due to Unintended Boom Movement
Altec is recalling 2021 AH125 aerial devices because a defective component may cause the boom to move unexpectedly, increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E006000·2022-02-03
Nexxpro Recalls X.R2 Motorcycle Helmets Due to Impact Protection Defect
Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V058000·2022-02-03
Altec Recalls 2017-2021 LS60 Aerial Devices Due to Bearing Bolt Risk
Altec is recalling 2017-2021 LS60 aerial devices because bearing bolt washers may interfere with welds, causing bolts to break and increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V054000·2022-02-03
Jayco Eagle Fifth Wheel Trailers Recalled for Ungrounded Electrical Box
Jayco is recalling 2022 Eagle fifth wheel trailers because the metallic electrical box may not be grounded, posing an electric shock risk.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V059000·2022-02-03
Class C Motorhomes Recalled for Defective Steering Bolts
Jayco is recalling certain 2021-2022 Entegra Coach Accolade and Jayco Seneca Class C motorhomes because steering arm and tie rod bolts may fracture, causing loss of steering control. Free replacement available.
Product
ENTEGRA — ENTEGRA, JAYCO ACCOLADE XL, SENECA PRESTIGE, SENECA, ACCOLADE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22719·2022-02-03
River Street Five-Drawer Chests Recalled for Tip-Over and Entrapment Hazards
BFG North Carolina is recalling about 1,380 River Street Five-Drawer Chests sold at Rooms To Go from February 2019 through October 2021. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children.
Product
River Street Five-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V057000·2022-02-03
Highland Ridge RV Recalls 2022 Olympia Models Due to Electrical Grounding Defect
Highland Ridge RV is recalling 2022 Olympia and Olympia Sport recreational vehicles because the metallic electrical box may not be grounded, posing a risk of electric shock.
Product
HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OLYMPIA, OLYMPIA SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V053000·2022-02-02
2021-2022 Jayco and Entegra motorhomes recalled for loose tie rod clamps
Jayco and Entegra are recalling certain 2021-2022 Class C motorhomes with loose tie rod clamps that could lead to steering loss and increased crash risk.
Product
JAYCO — JAYCO, ENTEGRA SENECA, ACCOLADE, ACCOLADE XL, SENECA PRESTIGE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0398-2022·2022-02-02
Cefuroxime Sterile Ophthalmic Injection Recalled Due to Sterility Concerns
Edge Pharma is recalling Cefuroxime sterile ophthalmic solution for injection because the company cannot assure the product meets sterility requirements. The recall affects approximately 1,720 syringes distributed nationwide.
Product
Cefuroxime, Sterile Ophthalmic Solution for Injection, Preservative Free, 3mg/0.3mL (10 mg/mL), 0.3 mL single use syringe for Intraocular Injection, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446 NDC 05446-1003-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0399-2022·2022-02-02
Dexamethasone Sodium Phosphate Otic Injection Syringes Recalled for Lack of Sterility Assurance
Edge Pharma LLC is recalling Dexamethasone sodium phosphate sterile otic solution for injection syringes (NDC 05446-0848-01) due to lack of assurance of sterility. Approximately 323 syringes were distributed nationwide.
Product
Dexamethasone sodium phosphate, sterile otic solution for injection Preservative free, 19.2 mg/0.8mL (24mg/mL), 0.8 mL per syringe Single Use Syringe For Otic Injection, Edge Pharma LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-0848-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0418-2022·2022-02-02
Phenylephrine Injection Recall Due to Sterility Assurance Concerns
Edge Pharma is recalling phenylephrine injection (20 mg/250 mL) because the manufacturer cannot assure the product maintains sterility. The recall affects 3,930 bags distributed nationwide.
Product
PHENYLephrine, 0.9% Sodium Chloride Injection, USP, 20 mg/250mL, (0.08 mg/mL), Single use bag for IV injection (Preservative Free), Rx Only, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT NDC 05446-1667-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0394-2022·2022-02-02
ALUM Concentrate IV Bags Recalled for Lack of Sterility Assurance
Edge Pharma, LLC is recalling ALUM Concentrate (Aluminum Potassium Sulfate Dodecahydrate) IV bags nationwide due to lack of assurance of sterility. The affected product is a prescription intravenous medication supplied in 300 ml bags.
Product
ALUM Concentrate (Aluminum Potassium Sulfate Dodecahydrate in Sterile Water (PF) 30 g/300 ml, IV bag, Rx Only, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-0637-03
Category
Drug
Distribution
Distributed nationwide