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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.

1,583 stored notices name South Dakota, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.

Medical devices

Reported Jan 4, 2023

Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acumed LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Companion Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Medical Systems, LLC

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intersect ENT, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 16, 2022

ReadyMeals Chicken Salad Quad, 12 oz., in a clear plastic container with four compartments, UPC 2 1352 40000 0,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Albertsons Companies LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 16, 2022

NaturaLyte Liquid Acid concentrate, Part Number 08-0231-4, four (4) one-gallon bottles per bottle case. For dialysis.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

iRhythm Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Sedecal Soltus Battery Mobile X-Ray System REF Soltus 450 Battery Mobile X-Ray System REF Soltus 500

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sedecal Sa

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2022

BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company, BD Biosciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bella Brands, LLC dba Bella Cucina Artful Food

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 9, 2022

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2022

THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 2, 2022

THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Chai Box

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 26, 2022

Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Vascular

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 26, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lyons Magnus LLC

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seeking Health LLC

FDA (openFDA food enforcement)

Food

Reported Oct 12, 2022

Sprigs - Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eden's Answers Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

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.