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 48,122 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported May 2, 2018
clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperVision Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
MicroVue CIC-C1q EIA, Model A001. An enzyme immunoassay for the detection of circulating immune complexes in human…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Cali Green Malay Kratom all packages, all quantities
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutrizone LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smucker Natural Foods, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended by ALL AMERICAN SEASONINGS, 10600 E. 54th Ave., Units B & C,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.All American Seasonings, Inc.
FDA (openFDA food enforcement)
Reported Apr 18, 2018
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
AUTO REF/KERATOMETER ARK-1s
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Normed Charcot Osteotome Chisel (Various sizes)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
FDA (openFDA device enforcement)
Reported Apr 11, 2018
2008 K2 Hemodialysis Machine with software version 5.40, Models: (1) Hemodialysis SYS OLC/Diasafe PLS 190610, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Reported Apr 11, 2018
CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO*…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Apr 11, 2018
Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Harvest, Inc.
FDA (openFDA food enforcement)
Reported Apr 11, 2018
diet Pepsi, 12 FL OZ, in aluminum cans packaged in 12 pk paper cartons
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pepsi Beverage Co.
FDA (openFDA food enforcement)
Reported Apr 11, 2018
Alpha Air 6 ENT Microscope Microscope examination of the human ear, nose, and throat.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seiler Instr. & Mfg. Co. Inc.
FDA (openFDA device enforcement)
Reported Apr 11, 2018
King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The King Arthur Flour Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 4, 2018
ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Konica Minolta Medical Imaging USA, Inc.
3 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.