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.
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)
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)
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)
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)
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)
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)
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)
Reported Oct 16, 2019
Clinical Chemistry, ABX Pentra Lipase CP, ABX Pentra 400/Pentrac400, REF: A11A01631, Model/Part # 1220001631, UDI #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Incorporated
FDA (openFDA device enforcement)
Reported Oct 16, 2019
K2M Special Connector Instruments (Special Connector, Special Adaptor, and Quick Adaptor) Product Usage: Special…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.K2M, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 100g; Ingredients: sugar,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stark Inc.
FDA (openFDA food enforcement)
Reported Oct 16, 2019
Tep Say Crispy Tiny Shrimp Snack, Net Wt. 7 oz. in plastic jar UPC 7 37483 77926 9 Distributed By: First World Trading…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vinh Sanh Trading Corp.
FDA (openFDA food enforcement)
Reported Oct 9, 2019
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2019
TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paltop Advanced Dental Solutions Ltd.
FDA (openFDA device enforcement)
Reported Oct 9, 2019
Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Hemospray Endoscopic Hemostat
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2019
Astrochef LLC. Retira Platos Preparados De Pollo Estilo Pub Debido A Un Error De Rotulación Y Alérgenos No Declarados
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pegasus Foods Inc.
USDA FSIS
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 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.