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.
Reported Apr 2, 2025
DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.U.S. Tov, Inc. dba U.S. Trading Company
FDA (openFDA food enforcement)
Reported Mar 26, 2025
BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2025
Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FUJIFILM Healthcare Americas Corporation
FDA (openFDA device enforcement)
Reported Mar 26, 2025
Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oridion Medical 1987 Ltd.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2025
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 11 mm, Product Code: 880-601/11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2025
CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 946 mL UPC 0 41271 01993 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone Wave
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2025
1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shearer's Foods, LLC
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Medical Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruAbutment Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Turkana Food Inc.
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZB Importing LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
BD BBL TB Stain Kit K, Catalog (REF): 212522
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for use in catheter based…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Biosense Webster, Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number: TBS iNsight v3.x / pn: OS-TBSi Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medimaps Group
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Paradigm REF: MMT-712 and MMT-715
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spicin Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 5, 2025
DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Laboratory Systems (suzhou) Co., Ltd.
FDA (openFDA device enforcement)
Reported Mar 5, 2025
BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
6 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.