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.

1,551 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.

Medical devices

Reported May 3, 2017

ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…

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

Orthosoft, Inc. dba Zimmer CAS

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…

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

Remel Inc.

FDA (openFDA device enforcement)

Food

Reported May 3, 2017

Raisin Bread, Valley Bakery, Rock Valley, IA, 1 count. UPC 290104404006, packaged in clear plastic bags

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

Valley Bakery Wholesalers Inc.

26 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…

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

Ashers Chocolates/Lewistown, Inc.

86 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…

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

Covidien Medtronic

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2017

LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797

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

Nonna Foods

FDA (openFDA food enforcement)

Food

Reported Apr 19, 2017

Miranda, 5 lb. wrapped in paper; Vulto Creamery, Walton, NY.

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

Tomales Bay Foods, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2017

Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general…

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

Windstone Medical Packaging, Inc.

17 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2017

BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…

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

Philips Medical Systems (Cleveland) Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2017

JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…

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

Data Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Hitachi Oasis MRI System

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

Hitachi Medical Systems America Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Raindrop Near Vision Inlay, Model# RD1-1

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

Revision Optics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call…

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

Stanley Security Solutions Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2017

BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

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

Medtronic

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2017

Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…

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

Cook Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

EliA Sample Diluent, Article number, 83-1023-01

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

Phadia US Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2017

Deep River Sour Cream & Onion Krinkle Kettle Chips 2 oz bag UPC 8 50668 00049 8 & 5 oz bag UPC 8 50668 00099 3

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

Shearers Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Mar 6, 2017

Rochester Meat Company Recalls Pork Sausage Products Due To Misbranding

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

Branding Iron Holdings

USDA FSIS

Medical devices

Reported Mar 1, 2017

ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2017

Chocolate almond bark packaged in 4 oz. (UPC 026133400000) and 12 oz. (UPC 021633300000) plastic tray containers for…

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

Hy-Vee Stores Inc.

7 more products in this recall

FDA (openFDA food 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.