All recall categories

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.

Food

Reported Dec 29, 2021

Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net Wt. 6.5 oz. UPC 37296-10100, Dakota Toms,…

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

Dakota Tom's, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 29, 2021

Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…

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

Activbody, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

API 50 CH, Model 50300

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 24, 2021

Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, item…

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

Bix Produce Company LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 24, 2021

Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…

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

Fujifilm Irvine Scientific, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Permobil TiLite, Models: Aero Z, and ZRA

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

TiSport, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 17, 2021

Hemodialysis Delivery System, Software Version 2.x.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 17, 2021

NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…

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

NOW Health Group Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 10, 2021

Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and…

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

Ivar's Commissary

FDA (openFDA food enforcement)

Food

Reported Nov 10, 2021

Hamburger buns, customer specified formula, in unlabeled clear plastic bags, 30 or 12 buns per bag.

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

Kansas City LLC., dba Best Harvest Bakeries

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 10, 2021

IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL…

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

Lumenis, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 3, 2021

Simply Nature Organic Poppy Seed Dressing

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

Schlotterbeck & Foss LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 3, 2021

REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery…

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

W L Gore & Associates, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051

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

DiaSorin Molecular LLC

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.