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.

3,918 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.

Medical devices

Reported May 18, 2022

The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…

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

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…

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

Daavlin Distributing Company

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case

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

Eastland Food Corporation

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Accula SARS-CoV-2 Test, REF: COV4100

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

Mesa Biotech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

TMJ Arthroscopy Drape, 85''x 96''

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

Microtek Medical Inc.

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5…

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

Power Selles Imports dba Culinary Collective

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model…

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

Proterixbio

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

FDA (openFDA device enforcement)

Food

Reported May 11, 2022

WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515…

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

Bakkavor Foods USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300…

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

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.via…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

TearCare version 1.0 SmartHubs

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

Sight Sciences, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010

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

Acumed LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…

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

DNA Genotek Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

Matrix Clinical Solution At-Home COVID-19 Test

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

Matrix Medical Network

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…

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

Respironics California, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

Merlin PCS 3650 programmer Model 3330 software

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

St. Jude Medical, Cardiac Rhythm Management Division

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 20, 2022

20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)

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

Abbott Vascular

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 20, 2022

Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case

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

B&G Foods North America, Inc.

FDA (openFDA food 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.