Recalls distributed in Utah
These notices name Utah 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.
2,860 stored notices name Utah, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Utah too — those are in the archive.
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)
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)
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)
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)
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)
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
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
Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyzer intended for clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Scientific N.V.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
BioEnvelope, surgical mesh envelope. Labeled as the following: 1. BioEnvelope (Medium) (single pack); 2. BioEnvelope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aziyo Biologics
1 more product 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
Popchips Sea Salt Potato Popped Chips; 5 oz. bag, 0.8 oz. bag UPC: 0 82666 50080 3 - 5 oz. ; UPC: 0 82666 71100 1 - 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonora Mills Foods Inc. dba Popch
3 more products in this recall
FDA (openFDA food 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
Gold Medal Enriched, Presifted, Unbleached All Purpose Flour, Net Wt. 5 lb (2.26 kg), in paper bags. UPC 16000-19610
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food 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
Espinaler Razor Clams (Trimmed) 4/6 Classic Line, " N4R-LE7R printed on the tin AND/OR E7R MM/YYYY printed on the box.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.YTM, Inc. dba A Priori Specialty Foods
FDA (openFDA food 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
FuPaiYuan "***NOUGAT CANDIES***20190424***Candy***NET WT 450G (15.8oz)***INGREDIENTS Glucose syrup, sugar, peanut,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2019
AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
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.