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 Feb 19, 2025
Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
FDA (openFDA device enforcement)
Reported Feb 19, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Max Mobility LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2025
SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BakeMark USA LLC.
FDA (openFDA food enforcement)
Reported Feb 5, 2025
BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Infinity Central Station. Model Number: MS26800 The Infinity CentralStation (ICS) is intended for centralized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2025
McKesson Cardiology Hemo software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.A L I Technologies Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
38 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wholesale Produce Supply LLC dba
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2025
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Unitek Corporation
FDA (openFDA device enforcement)
Reported Jan 8, 2025
Napoleonas Torte packaged under the following sizes: 1. Small, Net Wt 1.25 lbs. (sub ingredients contain wheat, yellow…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lithuanian Bakery, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 8, 2025
Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico. 2.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russ Davis Wholesale
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2025
BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Borsari Food Company Inc.
FDA (openFDA food enforcement)
Reported Jan 1, 2025
BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straight Smile, LLC
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
3 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.