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 Oct 18, 2023
Evivo with MCT Oil Infant Probiotic Activated B. infantis EVC001 (ActiBif) For Enteral or Oral Administration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Infinant Health, LLC
FDA (openFDA food enforcement)
Reported Oct 18, 2023
3T Heater Cooler System, REF: 16-02-85
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova Deutschland GmbH
FDA (openFDA device enforcement)
Reported Oct 18, 2023
CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RoyalVibe Health Ltd.
FDA (openFDA device enforcement)
Reported Oct 18, 2023
LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Little Oak Company Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 11, 2023
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Oct 4, 2023
1 lb. bags of CellarScience ascorbic acid, packaged in vinyl bags on 11/18/2022, Sku: AD615LB, Batch Number 56559, UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Moreflavor, Inc.
FDA (openFDA food enforcement)
Reported Oct 4, 2023
Dried Longans
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.SLR FOOD Distribution, Inc.
FDA (openFDA food enforcement)
Reported Sep 27, 2023
COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with four independent RF channels, allowing all RF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
DJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Great Lakes Cheese, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 23, 2023
Green Valley Foods Retira Productos Congelados De Pizza De Carne Debido A Un Error De Rotulación Y Alérgenos No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Green Valley Foods
USDA FSIS
Reported Sep 20, 2023
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2023
KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2023
La Reyna Diablo Salsa. Red Diablo Salsa, Hot. Product Code 1782. Net Wt 8 oz. UPC 7 52830-92710 0. Ingredients: Dried…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Twin Cities Co-Op Partners Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 13, 2023
ZVU Functional GI Software, REF: ZVU-3
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diversatek Healthcare
FDA (openFDA device enforcement)
Reported Sep 13, 2023
Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
FDA (openFDA food enforcement)
Reported Sep 13, 2023
ISee Ortho-K Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PARAGON VISION SCIENCES, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2023
3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter 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.