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 48,765 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.
Reported Feb 24, 2021
Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confirm Biosciences Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2021
System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2021
LumiraDx SARS-CoV-2 Ag Test Strip Kit US EUA (48 Tests / EN). LumiraDx Severe Acute Respiratory Syndrome (SARS) CoV-2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LumiraDx
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjohuntleigh Magog, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draegar Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 10, 2021
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Feb 3, 2021
B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Braxton Medical Corporation
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
32 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Frozen Ground Tuna, Wild Caught, Production Date: 06/01/2020. Product of Vietnam, Net Wt: 11 lbs. x 2: 22 lbs. Imported…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ocean Providence Minneapolis LLC
FDA (openFDA food enforcement)
Reported Jan 20, 2021
All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2021
FSIS Issues Public Health Alert for Not-Ready-to-Eat, Heat Treated, Not Fully Cooked Chicken Enchilada Products Due to…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Dec 30, 2020
MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ (396g) Canyon Bakehouse, LLC Johnstown, CO 80534 UPC 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods (Corporate Offices)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 30, 2020
Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Dec 30, 2020
42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Dec 16, 2020
MAC VU360, Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Hy-Vee, Short Cuts, Grill Ready Veggie Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hy-Vee Stores Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
1 more product 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.