Recalls distributed in Colorado
These notices name Colorado 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.
3,863 stored notices name Colorado, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported Dec 4, 2019
Ready to eat Pip Pop Movie Theater Popcorn packaged in 24 oz. laminated plastic zip pouch bag, 6 per case, UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Gardens Confections LLC
FDA (openFDA food enforcement)
Reported Dec 4, 2019
365 Everyday Value Organic Instant Oatmeal Maple and Brown Sugar Pecan With Other Natural Flavors UPC 9948247977 NET WT…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Whole Foods Market
FDA (openFDA food enforcement)
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
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
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Simplot simple goodness Classic Mixed Vegetables, foodservice item. There are 12/2.5 lbs. clear plastic bags per case.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simplot-Rdo LLC
FDA (openFDA food 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
Fire Roasted Medium Arriba! Bacon Salsa with Real Bacon NET WT 16 OZ. UPC Code: 033907 20513 1 packaged in a clear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Riba Foods Inc.
FDA (openFDA food 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
Kroger Wild Caught Sockeye Salmon Boneless, Frozen, Raw, Skin-on, not ready to eat (NRTE), individually vacuum packed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cold Locker Processing LLC
FDA (openFDA food 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
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
Autoject EI, REF AJ1310
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 7, 2019
Rastelli Bros., Inc. Retira Productos De Carne De Res Debido A Una Posible Contaminacin Con Materia Extraa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rastelli
USDA FSIS
Reported Nov 6, 2019
Various products which were contract sterilized.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Anewmed Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2019
AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules Rx Only NDC 42291-735-50 UPC 342291735507 Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVKARE Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 6, 2019
Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
C3 Wave App, v. 2.0.5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
1 more product in this recall
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
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
FDA (openFDA food 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.