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 Jan 1, 2020
Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fuji Food Products, Inc.
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2019
J&J Distributing Retira Productos De Ensalada Debido A Un Error De Rotulación Y Alérgenos No Declarados
High riskUsing this product could cause serious injury, illness or death — stop using it now.J&J Distributing
USDA FSIS
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Habib EUS RFA, 10mm electrode active tip, Material Number/UPN: 6500 - Product Usage: The Habib EUS RFA is indicated for…
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 18, 2019
Healix Knotless ADV BR 4.75 Suture Anchor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
41 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Klein Foods Cookie Dough Fudge, packed in 1/2 pound boxes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Klein Foods, Inc.
FDA (openFDA food enforcement)
Reported Dec 18, 2019
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Broccoli Cheddar Pasta Salad Kit V 1/3.7625 LBS Distributed By: Russ Davis Wholesale Wadena, MN 56482 UPC 1345435840…
High riskUsing this product could cause serious injury, illness or death — stop using it now.RMJV, LP dba Fresh Creative Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 18, 2019
Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Sullivan Harbor Farm Smokehouse Refrigerated, Ready-to-Eat, Cold Smoked Salmon in vacuum packaging (4 oz., 8 oz., 1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mill Stream Corp.
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Tuna King 4 oz. and 6 oz. Tuna Steaks (frozen) Production date 06/13/2019 Expiration: 06/13/2021 4 oz. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern Fisheries Ltd.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Theralase Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, 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.