State

South Carolina product recalls

73,118 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: 1,882
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 1,882 (26%) are Severe.

Which agencies issued them

These figures cover only the 7,145 recalls whose distribution notice names South Carolina specifically. The 73,118 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12401–12425 of 80263

HighFDA (Drugs)·D-0437-2024·2024-04-17
FDA Recalls Rifampin Capsules 300mg Nationwide for Subpotency
Lupin Pharmaceuticals recalls Rifampin Capsules USP 300mg nationwide due to subpotency—the drug contains less active ingredient than labeled. Affected lot: A201064, expiring March 2024. 26,352 bottles involved.
Product
Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V274000·2024-04-17
Toyota Prius Prime rear door opener switch water intrusion recall
Toyota is recalling 2023–2024 Prius and Prius Prime vehicles because water may enter the rear door switch, causing it to short circuit and allow the rear door to open unexpectedly while driving or during a crash.
Product
TOYOTA — TOYOTA PRIUS, PRIUS PRIME
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2024·2024-04-17
Femoral Resurfacing Cup Components Marketed Without Required FDA Clearance
Synovo Production recalled 496 femoral resurfacing cup components that were marketed without FDA clearance. These hip implant components were distributed in the United States.
Product
Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA SPRAY, STERILEEO, Reference Numbers: 01-03-0042 01-03-0044 01-03-0045 01-03-0047 01-03-0049 01-03-0051 01-03-0052
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2024·2024-04-17
EndoVive 20 Fr Feeding Tube May Obstruct During Placement
Boston Scientific is recalling EndoVive 20 Fr feeding tubes due to potential blockage during placement that may prevent guidewire advancement. This could lead to procedure complications including bleeding, gastric leakage, or aspiration.
Product
EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509191
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1488-2024·2024-04-17
Medline SwivAssist Bed Assist Bars Recalled for Safety Standard Non-Compliance
Medline is recalling 79 Bed Assist Bars that failed to comply with federal safety standards for adult portable bed rails. The products were manufactured after the compliance deadline.
Product
Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline SwivAssist Bar, Model Number MDS6800SWIVRH (individual)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0439-2024·2024-04-17
Prescription Drug Isotretinoin Recalled Due to Over-Potent Formulation
Teva Pharmaceuticals recalls Isotretinoin 40mg capsules for exceeding specification limits in potency. No illnesses reported.
Product
ISOTRETINOIN — ISOTRETINOIN (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1508-2024·2024-04-17
Nucleic Acid Isolation Device Recall: EZ2 Connect MDx-IVD Heater Failure
Qiagen Sciences is recalling 168 units of the EZ2 Connect MDx-IVD nucleic acid isolation device due to insufficient welding that causes heater cable embrittlement and device malfunction, resulting in sample loss during testing.
Product
EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model Number: 9003230
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V272000·2024-04-17
Forest River Travel Trailers LED Backlight Circuit Board Fire Risk
Forest River and Dynamax are recalling multiple 2018–2024 travel trailer models due to LED backlight circuit boards in cooktop ranges that may overheat and create a fire risk. Dealers will disconnect and remove the LED backlight wiring at no charge.
Product
FOREST RIVER — FOREST RIVER, DYNAMAX IBEX, DX3, CEDAR CREEK, WILDCAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2024·2024-04-17
PEG feeding tube with blocked connector may impede placement procedure
Boston Scientific's EndoVive 20Fr PEG Kit may have a blocked connector that prevents the guidewire from advancing during placement, potentially causing complications including bleeding and aspiration.
Product
EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00568211
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2024·2024-04-17
RayStation Software Use Error Could Cause Incorrect Radiation Dose Calculations
RayStation radiation therapy planning software versions 8B through 2024A contain a use error that can incorrectly select silicon material for silicone gel polymer implant dose calculations, potentially resulting in incorrect radiation doses.
Product
RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B, 2024A including some service packs.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1148-2024·2024-04-17
Deluxe brand Macarons Party Edition recalled for undeclared allergens
Lidl is recalling Deluxe Macarons Party Edition due to undeclared allergens. The packaging is labeled in a foreign language and does not identify wheat, soy, egg, milk, and tree nuts.
Product
Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic container
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-1497-2024·2024-04-17
Acetabular Bearing Components Recalled for Marketing Without FDA Clearance
Synovo Production is recalling 1,681 acetabular bearing components that were marketed without FDA clearance.
Product
ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2024·2024-04-17
da Vinci SP Surgical System Patient Cart Welds May Fail
Intuitive Surgical recalled 53 da Vinci SP Surgical System Patient Carts due to inadequate welds in the instrument arm joints. These welds may cause tissue injuries, conversion to open surgery, or user pinching injuries.
Product
Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
Category
Medical Device
Distribution
21 states
HighNHTSA·24V275000·2024-04-17
Lexus LS Air Bag Sensor May Fail to Detect Front Passenger
Toyota is recalling certain 2018–2021 Lexus LS and LS Hybrid vehicles with the Executive Package because the front passenger seat occupant sensor may fail to detect a passenger, risking improper air bag deployment in a crash.
Product
LEXUS — LEXUS LS, LS HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2024·2024-04-17
EndoVive 20Fr Push Safety PEG Kit Recall Due to Blocked Lumen Risk
Boston Scientific is recalling the EndoVive 20Fr PEG feeding kit due to blockage in the barb connector that can prevent proper placement. The blockage may lead to prolonged procedures, bleeding, gastric leakage, and aspiration risk.
Product
EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509011
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1138-2024·2024-04-17
Hashbrown Casserole Recalled Due to Missing Ingredient Labeling
Robeson Enterprises is recalling Pies & Sides Hashbrown Casserole because the label lacks an ingredient list, preventing consumers from identifying allergens. The product was distributed in Georgia, North Carolina, and South Carolina.
Product
PIES & SIDES HASHBROWN CASSEROLE, ALLERGENS: MILK, WHEAT, SOY, FISH, PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
HighFDA (Food)·F-1133-2024·2024-04-17
PIES & SIDES Broccoli Casserole Recalled for Missing Ingredient Labels
PIES & SIDES Broccoli Casserole by Robeson Enterprises is recalled because the product label does not list ingredients. The product contains wheat, eggs, milk, soy, and fish.
Product
PIES & SIDES Broccoli Casserole Contains: Wheat, Eggs, Milk, Soy, Fish PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1514-2024·2024-04-17
PEG Feeding Tube Kit Recalled for Blocked Lumen Preventing Guidewire Advancement
Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.
Product
EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509051
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1144-2024·2024-04-17
Squash casserole recalled for missing ingredient and allergen labeling
Robeson Enterprises is recalling its Pies & Sides squash casserole due to missing ingredient list labeling. The product contains undisclosed allergens (milk, eggs, soy, fish, wheat).
Product
PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FISH, WHEAT PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1146-2024·2024-04-17
Sweet Potato Casserole Recall Due to Missing Ingredient Labels
Robeson Enterprises is recalling Pies & Sides Sweet Potato Casserole because the product label fails to list any ingredients, including egg and milk. Consumers with allergies to these ingredients should not consume the product.
Product
PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1135-2024·2024-04-17
Caramel Apple Pie Recalled for Missing Sub-Ingredient Labels
Robeson Enterprises is recalling 2,984 units of Pies & Sides Connie's Caramel Apple Pie due to incomplete ingredient labeling. The product labels do not list sub-ingredients for prepared components.
Product
PIES & SIDES CONNIE'S CARAMEL APPLE PIE 11 oz INGREDIENTS: APPLE PIE FILLING, SUGARS, VANILLA, CARAMEL EXTRACT BLEACHED FLOUR, SPICES, CONTAINS: WHEAT, PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1145-2024·2024-04-17
Robeson Enterprises Recalls Strawberry Pie for Missing Sub-Ingredient Labeling
Robeson Enterprises is recalling Pies & Sides Strawberry Pie because the label fails to list sub-ingredients. Consumers with allergies cannot verify safe ingredients. The recall affects Georgia, North Carolina, and South Carolina.
Product
PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1134-2024·2024-04-17
Cherry Pie Recalled for Missing Sub-Ingredient Label Information
Robeson Enterprises is recalling cherry pie products because labels do not list sub-ingredients. Products were distributed in Georgia, North Carolina, and South Carolina.
Product
PIES & SIDES CHERRY PIE INGREDIENTS: CHERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR SPICES. CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0438-2024·2024-04-17
FDA Recalls Lansoprazole Delayed-Release Capsules for Manufacturing Practice Deviations
NATCO Pharma Limited is voluntarily recalling 30 bottles of Lansoprazole 15 mg delayed-release capsules due to Current Good Manufacturing Practice deviations. The product was distributed nationwide in the United States.
Product
Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1141-2024·2024-04-17
Peach pie recalled for missing sub-ingredient information
Robeson Enterprises is recalling Peach Pie distributed to GA, NC, and SC because the label fails to list sub-ingredients. The recall affects all lots shipped before February 23, 2024.
Product
PIES & SIDES PEACH PIE INGREDIENTS: PEACH PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states