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 Mar 13, 2024
The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2024
Taylor Farms Pacific Recalls Kroger Brand Ready-To-Eat Apple Walnut With Chicken Salad Bowl Products Due to Misbranding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farm - Pacific
USDA FSIS
Reported Mar 13, 2024
Cheese Enchiladas with Red sauce 4/pkg 14.5oz packaged in a in a Deep Meal tray Plant Fiber - Film 800.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Fierro Group Inc. dba Rico Brands
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2024
IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2024
GRAPHENANO DENTAL G-CAM, Product Codes: a) 95 Multichroma 14LB2, REF GC00089; b) 95 Multichroma 24LA2, REF GC00112; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Graphenano Dental Sl
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lakeview Farms LLC
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Neurosurgery
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2024
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
FDA (openFDA food enforcement)
Reported Feb 21, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2024
Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Tov, Inc.
FDA (openFDA food enforcement)
Reported Feb 21, 2024
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H787125004045, REF: 12500404; Pulse Spray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Sperm separation media are used to separate motile sperm from other constituents of semen.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Irvine Scientific, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
FLEXSelect 5/16" Amber Latex Elastics-Intended use is orthodontics, braces, tooth gap, Ref: AMD56
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G & H Wire Company
FDA (openFDA device enforcement)
Reported Feb 14, 2024
BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2024
Notoginseng Formula Special Gout Granule; 100% Natural; 8 G x 10 PACKS; CITI TRADE INT'L LIMITED; ADDRESS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.8th Ave Pharmacy
FDA (openFDA food enforcement)
Reported Feb 7, 2024
Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rizo Lopez Foods, Inc. dba Don Francisco Cheese
13 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 31, 2024
bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B-K Medical A/S
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Utah recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.