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 4, 2019
ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Tomato, Carrot, Broccoli & Snap Pea- 13 oz in clear plastic container. Brands: Crazy Fresh, Quick&Easy, or Plain Label
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russ Davis Wholesale, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2019
Missa Bay, LLC Recalls Salad Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay LLC
USDA FSIS
Reported Nov 20, 2019
Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galil Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
Schwan's Garlic Herb Shrimp NET WT 16 oz. (1 lb.) Keep Frozen Cook Thoroughly Distributed By: Schwan's Home Service,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fisherman's Pride Processor, Inc. dba Neptune Foods
FDA (openFDA food enforcement)
Reported Nov 13, 2019
StemPro¿ MSC SFM CTS"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2019
CardioLab/ComboLab Recording Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Simmons Prepared Foods, Inc. Retira Productos De Aves Debido A Una Posible Contaminación Con Materia Extraña
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simmons Prepared Foods, Inc.
USDA FSIS
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Posey Connected Twice-As-Tough Cuffs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tidi Products
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Andover Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Candela Corporation
3 more products in this recall
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.