State

South Carolina product recalls

73,388 recalls have nationwide distribution and so reach South Carolina. 7,145 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,145
Critical: 1,278
Severe: 2,166
Most recent: 2026-09-23

Of the 7,145 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 7,145 recalls whose distribution notice names South Carolina specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21401–21425 of 80533

HighFDA (Drugs)·D-1266-2022·2022-07-27
Morphine Sulfate Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC is recalling Morphine Sulfate Injection due to lack of assurance of sterility. The recall affects 8,985 syringes distributed nationwide.
Product
Morphine Sulfate Injection, USP, 30 mg/30 mL (1 mg/mL) syringe, packaged in 5 x 30 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1254-2022·2022-07-27
Glycopyrrolate Syringes Recalled Due to Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 3450 glycopyrrolate injection syringes (NDC 69374-903-30, Lot GL2004A) nationwide due to lack of assurance of sterility.
Product
Glycopyrrolate Injection, USP, 0.6 mg/3 mL (0.2 mg/mL) syringes, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-903-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1485-2022·2022-07-27
Honeymoons Milk Chocolate Cashew recalled for undeclared tree nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Cashew candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. Consumers with tree nut allergies face potential serious health risks.
Product
Honeymoons Milk Chocolate Cashew. PLU Code: 788394 14828 6
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1415-2022·2022-07-27
Medical Bed Mattress Microclimate Failure Increases Pressure Ulcer Risk
Affected Hill-Rom Centrella Pro+ hospital mattresses can fail to properly manage heat and moisture removal, increasing the risk of pressure ulcer development in patients.
Product
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1255-2022·2022-07-27
HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center recalled 22,805 pre-filled syringes of HYDROmorphone HCl Injection due to lack of sterility assurance. Six lot numbers were distributed nationwide.
Product
HYDROmorphone HCl Injection, USP, 10 mg/50 mL (0.2 mg/mL) syringes, 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th Street Extension, West Columbia SC 29172, NDC: 69374-529-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1457-2022·2022-07-27
Dark chocolate truffles recalled for undeclared tree nut allergens
Queen Bee Gardens is recalling Dark Mint Classic Truffles for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed to retail locations in CO, NM, WY and nationwide online.
Product
Dark Mint Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11035 1. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, dry milk, whey, agar, algin, lecithin & peppermint oil. Decoration: "Ivory" chocolate & artificial color.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1471-2022·2022-07-27
Honey Caramels Almond Coconut Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Almond Coconut due to potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Consumers allergic to tree nuts should not consume this product.
Product
Honey Caramels Almond Coconut. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz bag: 788394 12004 6. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, coconut, nonfat dry milk, whey, natural flavors, lecithin…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1424-2022·2022-07-27
Randox Cholesterol In Vitro Diagnostic Kits Fail Stated Performance Specifications
Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.
Product
Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1487-2022·2022-07-27
Chocolate Cashew Candy Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Cashew candy because it may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts, which can cause severe allergic reactions.
Product
Honeymoons Ivory Chocolate Cashew. PLU Code: 788394 14900 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1461-2022·2022-07-27
Queen Bee Gardens Huckleberry Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.
Product
Huckleberry Truffle. Net wt. 1.4 oz. PLU Code: 788394 11057 3. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], HONEY, "Ivory" chocolate (sugar, cocoa butter, whole & non-fat milk solids, sunflower…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1264-2022·2022-07-27
Lidocaine HCl injection syringes recalled due to sterility assurance failure
Nephron Sterile Compounding Center has recalled 37,310 syringes of Lidocaine HCl Injection USP 1% nationwide due to lack of assurance of sterility. Affected lots expire between August and October 2022.
Product
Lidocaine HCl Injection, USP 1%, 50 mg/5 mL (10 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-985-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1464-2022·2022-07-27
Bee Energy Bar recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Bee Energy Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.
Product
Bee Energy Bar. Net wt. 1.5 oz. PLU Code: 788394 18559 5. Ingredients: Dark chocolate (sugar, chocolate liquor, cocoa butter, milk fat [butter], sunflower lecithin, pure vanilla), honey, almonds, butter (pasteurized cream, salt), coconut, gluten free oats, dried…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1282-2022·2022-07-27
Aspirin-Dipyridamole Capsules Recalled for Capsule Breakage Defect
Glenmark Pharmaceuticals is recalling Aspirin and Extended-Release Dipyridamole Capsules due to capsule breakage defects. Approximately 168,936 bottles were distributed nationwide.
Product
ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE — ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE (ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1386-2022·2022-07-27
Stryker Trevo Trak 21 Microcatheter recalled for missing carton product illustration
Stryker Neurovascular is recalling 71 Trevo Trak 21 Microcatheter units because the product carton label is missing the required product drawing or illustration.
Product
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT 4X41+TRAK21 2-PACK - CE, REF: 91414; TREVO NXT 6X37+TRAK21 2-PACK - CE, REF: 91415; TREVO NXT 4X28+TRAK21+CAT6 3-PACK - CE…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1422-2022·2022-07-27
Laboratory Reagent Recalled Due to Inaccurate Calibration Curves
Randox Laboratories is recalling Soluble Transferrin Receptor reagent (TF10159) due to calibration curve defects causing inaccurate test results on Siemens Atellica CH analyzers.
Product
Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1423-2022·2022-07-27
Soluble Transferrin Receptor Calibrator Recall Due to Lab Errors
Randox Laboratories is recalling Soluble Transferrin Receptors Calibrator kits used in lab analyzers. The calibrators can produce incorrect test results, with some values potentially underestimated by up to 30 percent.
Product
Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1340-2022·2022-07-27
FDA Recalls Launch Sequence Euphoria Capsules as Unapproved Drug
Launch Sequence Euphoria Capsules were marketed without FDA approval. Consumers should discontinue use immediately and contact the manufacturer.
Product
Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC Code 661020846864.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1244-2022·2022-07-27
OTC Hydrogen Peroxide Solution Recalled for Isopropyl Alcohol Contamination
Vi-Jon's hydrogen peroxide topical solution has been recalled due to cross-contamination with low levels of isopropyl alcohol. Multiple brands are affected nationwide in the USA and Canada.
Product
HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1394-2022·2022-07-27
Triton Sponge System Software Instructions Updated for Proper Sponge Handling
Stryker is updating the Instructions for Use for the Triton Sponge System software (versions 4.6.5, 4.8.7, 4.9.6) to clarify proper handling technique for sponges and calibration placard. The FDA Class III recall affects 51 units distributed nationwide.
Product
Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1390-2022·2022-07-27
Erythropoietin Control Product Instructions Contain Incorrect CE Marking
R & D Systems is replacing Instructions for Use (IFU) for Quantikine IVD Erythropoietin Human Serum Controls due to an incorrect CE marking designation that should not appear on the self-certified product.
Product
Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1393-2022·2022-07-27
NeuRx Diaphragm Pacing System Labeling Revised for Storage Clarity
Synapse Biomedical revised labeling for the NeuRx Diaphragm Pacing System to clarify that temperature range symbols indicate storage conditions, not transport or package conditions. The revision affects 71 units distributed in the United States.
Product
NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036 NeuRx Diaphragm Pacing System, Patient Kit, SCI 20-0028 NeuRx DPS Surgical Kit, HDE 20-0040 NeuRx Diaphragm Pacing…
Category
Medical Device
Distribution
19 states
SevereNHTSA·22V539000·2022-07-26
Spartan Fire Recalls 2020-2021 Metrostar and Gladiator Trucks for Fire Risk
Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.
Product
SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V537000·2022-07-26
Capacity Recalls 2021-2022 TJ Trucks for Steering Gear Fracture Risk
Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.
Product
CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V538000·2022-07-26
E-One Fire Trucks Recalled for Electrical Connection Overheating Risk
E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.
Product
E-ONE — E-ONE CYCLONE II, TYPHOON, TYPHOON N, CYCLONE N
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V536000·2022-07-26
Ferrari Recalls Multiple Models Due to Brake Fluid Reservoir Cap Defect
Ferrari is recalling various models from 2005-2022 because a defective brake fluid reservoir cap may cause a leak, leading to partial or total loss of brake function.
Product
FERRARI — FERRARI CALIFORNIA, LAFERRARI, LAFERRARI APERTA, 612 SCAGLIETTI
Category
Vehicle
Distribution
Distributed nationwide