Recalls distributed in South Carolina
These notices name South Carolina in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
3,219 stored notices name South Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Sep 2, 2020
Whole Foods Market Buttermilk Biscuits, 4pk NET WT 1lb 0 oz PLU: 30561 packaged in plastic clam shell
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
HAVEN'S KITCHEN***GOLDEN TURMERIC TAHINI***NET WT 5oz (142g)***Ingredients: Water, Tahini, Extra Virgin Olive Oil,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Haven'S Kitchen
FDA (openFDA food enforcement)
Reported Aug 26, 2020
HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3 oz***KEEP FROZEN***10004302***PRODUCT OF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.High Liner Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal / Pediatric Oxygenators, Model Number: 701047495 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Tibial knee prosthesis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Sweeteeth O-Snap! (White Chocolate & Ginger Snaps) Chocolate Bar, NET WT. 3 OZ. (85.05G), Manufactured by: Sweeteeth…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sweeteeth Chocolate LLC
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellements LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sutter Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Aug 5, 2020
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2020
JBS Food Canada ULC Recalls Raw Boneless Beef Products Distributed without Benefit of Import Re-inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Balter Meat Company
USDA FSIS
Reported Jul 29, 2020
Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2020
syngo.via RT Image Suite with software versions syngo.via VB30 or VB40
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Walker Emulsions Hand Sanitizer (60%), Non-Sterile Solution, Alcohol Antiseptic 60%, 1 Gallon, Topical Solution, Walker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Walker Emulsions Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 29, 2020
LoFric Origo, Nelaton, 16in, FR10 urinary catheters
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wellspect HealthCare (Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.