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 Jul 1, 2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jul 1, 2026
6/11oz Sunflower Seeds Salted
High riskUsing this product could cause serious injury, illness or death — stop using it now.George J Howe Company, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2026
Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
INZONE DETACHMENT SYSTEM, REF: M00345100950
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 1, 2026
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Foods, LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 25, 2026
Reser’s Fine Foods, Inc. Recalls Ready-To-Eat Pasta Salad Product Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods
USDA FSIS
Reported Jun 24, 2026
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arrow International, LLC
34 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Jun 24, 2026
iLet Bionic Pancreas, REF: BB1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Mito Red Light, Super Mobile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mito Red Light Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutrisystem Inc.
FDA (openFDA food enforcement)
Reported Jun 24, 2026
Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical AG
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United States Bakery
FDA (openFDA food enforcement)
Reported Jun 17, 2026
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2026
EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berlin Heart GmbH
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kettle Cuisine, LLC
FDA (openFDA food enforcement)
Reported Jun 17, 2026
Farm Rich Pizza Cheese Crunchers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
FDA (openFDA food enforcement)
Reported Jun 17, 2026
DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.U.S. Tov, Inc. dba U.S. Trading Company
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
2 more products in this recall
FDA (openFDA device enforcement)
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Other states
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.