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.
3,918 stored notices name Colorado, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported Nov 25, 2020
VNS Therapy¿ AspireSR¿ Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-Tech USA
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 18, 2020
SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesthetics Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epitope Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Nov 18, 2020
J&O Mixed Veggie Cup with Dip, Net Weight 5.0 oz. (128 g), UPC 95631-85818. Mfg By: RDW, Pueblo CO 81001
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russ Davis Wholesale, LLC
FDA (openFDA food enforcement)
Reported Nov 18, 2020
Niobe ES System, Models 001-006000-1 and 001-006100-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stereotaxis Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 11, 2020
metformin HCL ER 500 mg, a) 30 tablets NDC: 72789-009-30; b) 60 tablets NDC: 72789-009-60; c) 90 tablets NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 4, 2020
Instructions For Use document of the GPS Trackers.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Ortho
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Equinoxe Platform Fracture Stem, 6.5mm, Left - Product Usage: The Equinoxe Platform Fracture Stem is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hadson (Toko) Trading Co., Inc.
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Merge LIS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nurture Inc. dba Happy Family
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 4, 2020
5.5MM Arthrogarde Hip Access Cannula
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.eVenus Pharmaceutical Laboratories
FDA (openFDA drug enforcement)
Reported Oct 28, 2020
High Quality Organics Organic Parsley, Medium, Organic Parsley Fines 50 lbs. 25 lbs. 20 lbs. 0.25 lbs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Quality Organics
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 28, 2020
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
98 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Invivo Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
40 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.