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 48,122 notices were distributed nationwide, so they reach Colorado too — those are in the archive.

Medical devices

Reported Feb 27, 2013

LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage…

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

DePuy Orthopaedics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

HealthTronics Endocare 3.8mm RenalCryo Cryoprobe, R3.8L. The Endocare CryoProbe is an accessory probe intended for use…

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

Healthtronics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

Maquet ELS Cannula 15 FR. Used for extracorporeal membrane oxygenation (ECMO) for the treatment of respiratory…

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Food

Reported Feb 27, 2013

Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…

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

Nestle USA

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2013

Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2013

GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The T-piece Resuscitation System [ventilator, emergency…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2013

Stringless Sugar Snap Peas, Sunny Shores' Mann's. Net Wt 8 oz (227 g); Perishable, Preservative Free, keep…

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

Mann Packing Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2013

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

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

Mizuho OSI

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2013

Pamela's Baking and Pancake Mix; Gluten Free, Wheat Free 24 oz package. UPC 93709-30010 Pamela's Products, Ukiah, CA…

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

Pamela's Products, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2013

St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…

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

St Jude Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…

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

Diagnostic Hybrids Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Li-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400. Also branded as Reliability Plus byDrive.…

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

Oxus America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…

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

Synthes USA HQ, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…

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

Cordis Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774…

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

EonNutra, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt.…

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

Jiffy Food Service, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100. VITROS¿ Vapor…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general…

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

Philips Healthcare Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 23, 2013

Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink.…

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

Ocean Beauty Seafoods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 23, 2013

Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented…

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

Quanta System, S.p.A.

2 more products in this recall

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.