Recalls distributed in Minnesota
These notices name Minnesota 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.
3,845 stored notices name Minnesota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.
Reported Dec 18, 2024
Whole and Cut Cucumbers packaged in the following sizes: 1. Select 40-45 lb. boxes Item 05000. 2. Bix 1/5 lb. Item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sysco Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cartiva, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2024
Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g) Plastic Container with UPC# 193968044268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cedar's Mediterranean Foods, Inc.
FDA (openFDA food enforcement)
Reported Dec 11, 2024
AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dyma Brands
20 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279407074 and Case…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Jose Madrid Salsa Chipotle Con Queso, Net Wt. 13 oz. (369g), packaged in glass jars; 12 jars per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Michael Zakany LLC
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 11, 2024
BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2024
AMS Artificial Urinary Sphincter Control Pump
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 Dec 4, 2024
Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Curio Spice Co.
FDA (openFDA food enforcement)
Reported Dec 4, 2024
V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kci USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2024
Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroSurgical Technology Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2024
VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2024
Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Corp. Analytical & Measuring Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Chicken Alfredo Kit
High riskUsing this product could cause serious injury, illness or death — stop using it now.Joseph Seviroli, LLC
FDA (openFDA food enforcement)
Reported Nov 27, 2024
Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Product Technology Center - Nestle Health Science
FDA (openFDA food enforcement)
Reported Nov 20, 2024
The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological sponges for use in the protection of neural tissue during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Surgical Company, LLC
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.