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.

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

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

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2025

BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients…

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

Philips Respironics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

ADVIA¿ 120/2120/2120i SETpoint Calibrator

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

Siemens Healthcare Diagnostics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY

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

Becton Dickinson Infusion Therapy Systems, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number:…

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

Encore Medical, LP

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Spectral CT. Computed tomography X-ray system.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…

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

Balt USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2025

Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper…

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

Yerba Prima Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2025

LOWER EXTREMITY, Model: NCEX20I; LOWER EXTREMITY, Model: NCEX20J; TOTAL KNEE PACK, Model: NCTK31K; TOTAL KNEE PACK,…

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

American Contract Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…

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

Bd Switzerland Sarl

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2025

Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode#…

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

Comvita USA Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2025

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL.…

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…

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

Microtek Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

iBOT PMD with software version 01.05.24. Personal Mobility Device.

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

Mobius Mobility LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box)…

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2025

Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Oats and Honey. Net Wt 48 oz (3 lbs) 1.36kg. 2 Bags…

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

Post Consumer Brands, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 11, 2025

Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…

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

Beckman Coulter Mishima K.K.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2025

GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…

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

GNC Holdings LLC

FDA (openFDA food enforcement)

Food

Reported Jun 11, 2025

Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case

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

Nordic Naturals, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 4, 2025

Apo B Reagent, REF: OSR6143

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

Beckman Coulter Ireland, Inc.

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.