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.
2,917 stored notices name Utah, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Utah too — those are in the archive.
Reported Jun 21, 2017
L.A. LUCKY BRAND SWEET BASIL SEEDS: Hot E 2.1 OZ (60 G) BAGS; 100 BAGS PER CASE; Product of Vietnam. Ingredients: Sweet…
High riskUsing this product could cause serious injury, illness or death — stop using it now.L.A. Lucky Import & Export
FDA (openFDA food enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Arsenal Spinal Fixation System, Set Screw, Part No. 47027 Product Usage: The Arsenal Spinal Fixation System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola…
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Sun Dry Foods
FDA (openFDA food enforcement)
Reported Jun 14, 2017
Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt. 14 ounce. Retail package UPC 0 43301 61119 3.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lamb Weston Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2017
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Opteryx Variable Rescue Screw, Part #CP2214, UDI: *+M711CP22140/$$801716012*. Packaged in heat-sealed plastic bag.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovasis, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Microfixation, LLC
FDA (openFDA device enforcement)
Reported May 24, 2017
GIZA Vertebral Body Replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eden Spine Europe SA
FDA (openFDA device enforcement)
Reported May 24, 2017
WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2017
Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2017
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2017
Foster Poultry Farms Recalls Frozen Ready-To-Eat Breaded Chicken Patty Products Due to Possible Foreign Matter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Case Farms, Processing
USDA FSIS
Reported Apr 26, 2017
INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ace Surgical Supply Co., Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
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.