Recalls distributed in South Dakota
These notices name South Dakota 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.
1,551 stored notices name South Dakota, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.
Reported Jun 10, 2026
Atlan A350. Model Number: 8211500. anesthesia workstation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 10, 2026
1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Coffee Connexion Co., Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 20, 2026
Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produced in Winner, SD. Packaged in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dakota Honey Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 20, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dexcom, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…
High riskUsing this product could cause serious injury, illness or death — stop using it now.French Broad Chocolate Factory
FDA (openFDA food enforcement)
Reported May 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Innovations, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Europe Ltd.
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2026
Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2026
Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Apr 15, 2026
Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2026
SIGNA Premier systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2026
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
13 more products in this recall
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.