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.

3,919 stored notices name Colorado, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Colorado too — those are in the archive.

Medical devices

Reported Jul 29, 2015

Ring Transjugular Intrahepatic Access Set Product Usage: The Ring Transjugular Intrahepatic Access Sets are intended…

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

Cook Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…

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

DePuy Orthopaedics, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

iovera 155 Smart Tip; Catalog numbers:STT0412-10 and STT0412-5 (10 and 5 count respectively) iovera Smart Tips are…

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

Myoscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in…

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

Silhouette Lift, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…

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

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 23, 2015

Brown Packing Recalls Veal Products Due To Possible E. Coli Contamination

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

Brown Packing

USDA FSIS

Medical devices

Reported Jul 22, 2015

Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on…

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

Alere Scarborough, Inc. dba Binax, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…

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

Dr. Pepper Snapple Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2015

Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific…

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

Musculoskeletal Transplant Foundation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

Sorin Stockert Heater-Cooler 3T, 230 V Temperature control for extracorporeal perfusion of durations up to 6 hours.

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

Sorin Group USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Natural Grocers Caribbean Fruit & Nut Mix, Net Wt. (10 oz) (283g), packaged in plastic bag.

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

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Jul 15, 2015

Murry's, Inc., Recalls Chicken Products Due to Staphylococcal Enterotoxin Contamination

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

Murry's, Inc.,

USDA FSIS

Medical devices

Reported Jul 8, 2015

Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…

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

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models…

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

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

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

Tecan US, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Velocity" Biopsy Valve, 25 units per box, Product Usage: The disposable Velocity biopsy valve is used to cover the…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 3, 2015

Lombardi Brothers Meats Recalls Steak and Ground Beef Products Due To Possible E. Coli O157:H7 Contamination

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

Lombardi Brothers Meats

USDA FSIS

Food

Reported Jul 1, 2015

BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)

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

Blue Bell Creameries, LP

285 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

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

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch,…

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

Crystal Fresh

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.