State

South Carolina product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23676–23700 of 80649

SevereFDA (Drugs)·D-0630-2022·2022-02-23
THE RED PILL EXTRA STRENGTH Capsules Recalled for Undeclared Tadalafil
THE RED PILL EXTRA STRENGTH 800 mg capsules are being recalled because they contain undeclared tadalafil, an active ingredient in FDA-approved sexual-enhancement medications. The product was marketed and distributed as an unapproved drug nationwide via Amazon.
Product
THE RED PILL, EXTRA STRENGTH capsules, 800 mg, packaged in 10-count blisters packaged in a carton, ASIN B0847BSQQ5, Barcode X002G5GMJ1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0627-2022·2022-02-23
Arrow-Trerotola Percutaneous Thrombolytic Device catheter tips may separate during use
The FDA is recalling Arrow-Trerotola Percutaneous Thrombolytic Device catheters due to reports of tip separation during use. Approximately 3,668 units were distributed worldwide.
Product
Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0562-2022·2022-02-23
MAC DADDY RED Capsules Recalled for Undeclared Drug Ingredients
MAC DADDY RED Capsules are being recalled because they contain undeclared tadalafil and/or sildenafil without FDA approval. The product was distributed nationwide via Amazon Marketplace.
Product
MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0622-2022·2022-02-23
Vyaire Medical Ventilators Recalled Due to Potential Ventilation Failure
Vyaire Medical is recalling 4,189 bellavista 1000 and 1000e ventilators worldwide due to potential cessation of ventilation under specific conditions. This FDA Class I recall poses serious risk to patients who depend on these critical care devices.
Product
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista 1000/1000e ventilator is intended to provide positive pressure ventilatory support to adult and pediatric patients, and optionally, infant and neonatal patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0626-2022·2022-02-23
Arrow-Trerotola Percutaneous Thrombolytic Device Kits Recalled for Tip Separation
Teleflex is recalling Arrow-Trerotola Percutaneous Thrombolytic Device kits worldwide due to reports of tip separation during use, affecting approximately 1,874 units.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-65709-C, PT-03009, PT-65709-HS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0568-2022·2022-02-23
RNAstill Specimen Collection Kits Recalled Missing FDA 510(k) Clearance
BASE 10 GENETICS INC is recalling RNAstill Molecular Transport Medium Vials and specimen collection kits nationwide because they lack FDA 510(k) clearance. Approximately 455,791 kits were distributed across 18 states.
Product
RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of RNAstill MTM specimen collection kits: MTM-SW03 with Oropharyngeal swab and MTMSW-05 with Nasopharyngeal swab, packaged 25 specimen collection kits per plastic…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0624-2022·2022-02-23
Teleflex Arrow-Trerotola Percutaneous Thrombolytic Device PTD Kit recalled for tip separation
Teleflex recalls approximately 1,400 Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) kits due to reports of tip separation during use. The medical device is used for dialysis graft declotting and has been distributed worldwide.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0643-2022·2022-02-23
Paragard T380A Intrauterine Contraceptive Device Recall for Non-Sterility
CooperSurgical, Inc is recalling 48,645 cartons of Paragard T380A intrauterine contraceptive devices nationwide due to non-sterility concerns. The voluntary recall affects Lot #517001 with expiration date 1/2024.
Product
PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0631-2022·2022-02-23
365 SKINNY High Intensity Capsules Recalled for Undeclared Sibutramine
Je Dois Lavoir LLC is recalling 365 SKINNY High Intensity Capsules (600 mg, 30-count bottles) because the product contains undeclared sibutramine, a drug previously withdrawn from the US market due to safety concerns.
Product
365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0628-2022·2022-02-23
Arrow-Trerotola Thrombolytic Catheter Kits Recalled for Tip Separation During Use
Teleflex Medical is recalling 5,530 Arrow-Trerotola PTD catheter kits due to reports of tip separation during use. The hazard could prevent the device from functioning properly to remove blood clots from dialysis access grafts.
Product
5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-03000, PT-65509-S (PT-65509-S2 alternative), PT-01000-D (PT-01000-D2 alternative) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0629-2022·2022-02-23
Arrow-Trerotola Percutaneous Thrombolytic Device Set Tip Separation Recall
Teleflex Medical Inc. is recalling Arrow-Trerotola PTD catheter sets due to reported tip separation during use. The device is used for mechanical declotting of vascular access fistulae and grafts.
Product
Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV)…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0625-2022·2022-02-23
Arrow-Trerotola Dialysis Catheter Recalled for Tip Separation During Use
Arrow-Trerotola Over-The-Wire PTD catheters used in dialysis procedures are being recalled due to reports of tip separation during use. The FDA classified this as a Class I recall affecting 1,265 units worldwide.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0623-2022·2022-02-23
Arrow-Trerotola Thrombolytic Device Tip Separation During Use Recalled
Teleflex Medical is recalling Arrow-Trerotola PTD kits due to reports of tip separation during use. The affected device is used for declotting dialysis grafts and fistulae.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0653-2022·2022-02-23
Smiths Medical Medfusion Syringe Infusion Pumps Recalled for Alarm System Failures
Smiths Medical is recalling certain Medfusion syringe infusion pumps due to intermittent alarm system failures that may occur during power-on self-tests outside the warranty period.
Product
Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced during the same time period in which a main board was replaced using replacement main board part numbers G6000361, G6000435, G6001260, G6001560, G6001562 and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0735-2022·2022-02-23
Frozen Chopped Spinach Recalled for Possible Listeria Contamination
Steamable by Lidl Chopped Spinach is recalled due to possible Listeria monocytogenes contamination. Affected products were distributed to Lidl stores across eight states.
Product
Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-0642-2022·2022-02-23
Dental Resin Product Recalled Due to Non-Registered Manufacturing and Mislabeling
Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.
Product
FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0638-2022·2022-02-23
Endoscope Reprocessor Tubing Assembly Error May Reduce Disinfection Effectiveness
Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.
Product
OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes, their accessories, and endoscope reprocessor accessories
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0640-2022·2022-02-23
Liko Mobile Patient Lifts Recalled for Missing Bushings and Wear Risk
Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22087·2022-02-23
Bebe au Lait Wooden Teethers Recalled for Choking Hazard
Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.
Product
Wooden Teethers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V105000·2022-02-23
2022 Keystone Cougar Tires: Load Range Defect Increases Crash Risk
Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.
Product
KEYSTONE — KEYSTONE COUGAR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0639-2022·2022-02-23
Liko M220 mobile lifts recalled for missing bushing, fall risk
Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E013000·2022-02-23
Comoto Recalls Bilt Motorcycle Helmets for Impact Protection Defect
Comoto is recalling specific Bilt motorcycle helmets that may not adequately protect the wearer during a head impact, failing federal safety standards.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22086·2022-02-23
Festive Lights Hanukkah Menorahs Recalled Due to Fire Hazard
The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.
Product
Festive Lights Hanukkah Menorahs
Category
Consumer Product
Distribution
Distributed nationwide
ModerateNHTSA·22V102000·2022-02-23
Audi Recalls 2022 RS 5 Models for Incorrect Tire Loading Label
Audi is recalling 2022 RS 5 vehicles because the B-pillar tire and loading label displays an incorrect maximum weight, which may lead to vehicle overload.
Product
AUDI — AUDI RS 5
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0565-2022·2022-02-23
Alprazolam Tablets 0.5 mg Recalled Due to cGMP Deviations
ANI Pharmaceuticals is voluntarily recalling Alprazolam Tablets USP 0.5 mg in multiple package sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 205,662 bottles distributed across the United States.
Product
Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC 67253-901-50), and c) 1000-count bottles (NDC 67253-901-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Category
Drug
Distribution
Distributed nationwide