All recall categories

Recalls distributed in North Dakota

These notices name North 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.

1,377 stored notices name North Dakota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach North Dakota too — those are in the archive.

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens:…

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

Rayner Intraocular Lenses Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and…

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

Changzhou Biomet Medical Devices Co., Ltd.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…

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

Albertsons Companies LLC

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 22, 2022

Egg &Cheese Curd Snack/Power Box. Cheese Curds, Hard-Cooked Egg, Apple Wedges, Peanut Butter & Lettuce. Keep…

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 Jun 22, 2022

Drager SafeStar 55, Catalog No. MP01790

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2022

Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as a multi-chamber washer-disinfector for the washing,…

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

Getinge USA Sales Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2022

Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.

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

The TJX Companies, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 8, 2022

In-Line ventilator adaptor

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

Baxter Healthcare Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2022

BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically…

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

Becton, Dickinson and Company, BD Biosciences

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2022

JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…

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

The JM Smucker Company LLC

23 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 8, 2022

Jason & Mary Large Milk Peanut Butter Cup

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

Walnut Creek Chocolate Co. Inc.

14 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2022

Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…

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

Medtronic Neuromodulation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on…

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

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

AC-powered adjustable medical beds with built-in electric DC actuators and controls.

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

Umano Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

MicroScan WalkAway-40 plus Instrument REF B1018-283

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

Beckman Coulter Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Accula SARS-CoV-2 Test, REF: COV4100

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

Mesa Biotech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, 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.