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 Aug 26, 2020
Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2020
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellements LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Kouign-Amann Pastry available in plastic clamshell 4-packs with Whole Foods Market scale labels, a PLU code 26739400000
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
SUTUREFIX ULTRA Suture, Product number 72203855
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sutter Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Aug 5, 2020
1. FRESH CLAW AND KNUCKLE MEAT, 1 and 2 lbs. 2. FRESH CLAW, KNUCKLE, AND TAIL MEAT, 1 and 2 lbs 3. FROZEN CLAW AND…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greenhead Lobster Products
FDA (openFDA food enforcement)
Reported Aug 5, 2020
Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Aug 5, 2020
Smith & Nephew T-F1X0 RCG Drill Pac, 2 mm Drill & (2) Sleeves - Product Usage: indicated for use in surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2020
BodyGuard BodySet, REF: A120-160SAS
High riskUsing this product could cause serious injury, illness or death — stop using it now.CME America, LLC
36 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Mucocutaneous Swabs Product Usage: is intended for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Jul 22, 2020
***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kind LLC
FDA (openFDA food enforcement)
Reported Jul 22, 2020
ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Kinetics, LLC
44 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusion urodynamic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Laborie Medical Technologies, Canada Ulc
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
21 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.