All recall categories

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.

Medical devices

Reported Apr 1, 2020

RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Whole Foods Market Green Chile Chicken Tamale served as a Family Meal, Chef's Case, Packaged, Frozen and on he hot bar…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aesculap Implant Systems LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dreyers Grand Ice Cream, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ARJOHUNTLEIGH POLSKA Sp. z.o.o.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medicrea International

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

FilmArray NGDS Warrior Panel, Ref: NGDS-ASY-0007, UDI: (01)00851458005136, IVD, Rx Only

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Biofire Defense

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Blendtopia Products, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Driscoll's Raspberries- 6 oz. clamshell container 12 x 6 oz. per crate and 6 x 12 x 6 oz. (2 - 6 oz. attached…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Driscoll's Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

Monitor for the Functional Imaging System for Magnetic Resonance Imaging System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seca

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.