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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.

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)

Medical devices

Reported Oct 23, 2019

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…

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

ICU Medical Inc.

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2019

Cerelink ICP Monitor, Model Number 826820; intended for use as an interface between compatible strain-gauge type…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2019

Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the…

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

Roche Diagnostics Operations, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 23, 2019

Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG. CORP., Gardena, CA 90248 NDC…

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

Spectrum Laboratory Products

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 16, 2019

BD FACSLyric Flow Cytometer, 2-Laser 4 Color Instrument, REF: 662875, when using BD Trucount Tubes

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

Becton, Dickinson and Company, BD Biosciences

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 16, 2019

Madrona Market Delicatessen Hot Cocoa Mix, Net Wt. 2 lb (907 g), Distributed by Food Services of America, Inc.…

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

Diamond Crystal Brands Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 16, 2019

STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product code: SXPP1B430 suture

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

Ethicon, Inc.

1 more product in this recall

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.