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.
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in conjunction with bicarbonate in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medivators, Inc.
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 9, 2021
Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boehringer Ingelheim Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 2, 2021
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 26, 2021
REF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741045094 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported May 26, 2021
ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hi Tech Pharmaceuticals
13 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2021
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Public Goods
FDA (openFDA food enforcement)
Reported May 26, 2021
Veggie Pizza sold under the following brands: Crazy Fresh, quick & easy, and blank label. Item # 81068, Net Wt. 6.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Russ Davis Wholesale Inc.
FDA (openFDA food enforcement)
Reported May 19, 2021
REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
25 more products in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported May 19, 2021
ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St. Jude Medical, Cardian Rhythm Management Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 12, 2021
Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natrol, LLC
FDA (openFDA food enforcement)
Reported May 5, 2021
Power Wheelchair
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merits Holdings Co. dba Merits Health Products, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 5, 2021
Tuscan Garden Ranch Dressing, packaged in 16 oz bottles, Dist. & Sold Exclusively by ALDI, Batavia, IL packaged in 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richelieu Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 28, 2021
Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 28, 2021
KeVita Cucumber Rosemary (primary package), 15.2 oz., glass bottles, 6 packages per case, refrigerated storage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropicana Products, Inc.
FDA (openFDA food enforcement)
Reported Apr 21, 2021
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hollister Incorporated
FDA (openFDA device enforcement)
Reported Mar 31, 2021
BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 31, 2021
In-View Clear Leggings Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 31, 2021
RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 17, 2021
PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
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.