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 Nov 6, 2019

Various products which were contract sterilized.

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

Anewmed Corporation

FDA (openFDA device enforcement)

Drugs

Reported Nov 6, 2019

AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules Rx Only NDC 42291-735-50 UPC 342291735507 Manufactured…

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

AVKARE Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 6, 2019

Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

C3 Wave App, v. 2.0.5

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…

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

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…

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

Pajunk GmbH

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…

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

Dole Packaged Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software…

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

Life Technologies Holdings Pte Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix. Packaged in 13 oz (380 g) sealed plastic bags with paper…

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

The Truck Farm, LLC

FDA (openFDA food enforcement)

Food

Reported Oct 30, 2019

Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for:…

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

Threshold Enterprises Ltd.

FDA (openFDA food enforcement)

Food

Reported Oct 30, 2019

Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base, 435G SK, UPC 074410455200 Distributed by…

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

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 23, 2019

Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By: Arcadia Trading Inc. Brooklyn, NY 11211. USA…

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

Arcadia Trading Inc.

FDA (openFDA food enforcement)

Drugs

Reported Oct 23, 2019

Ascorbic Acid Sterile Injection Solution, 500 mg/mL, 50 mL vial, Non-Corn Source, Rx only, Atlas Pharmaceuticals, LLC,…

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

Atlas Pharmaceuticals, LLC

FDA (openFDA drug enforcement)

Free recall alerts

Get alerted about new Colorado recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.