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 48,122 notices were distributed nationwide, so they reach Utah too — those are in the archive.
Reported Sep 21, 2016
Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg. Urinary Health. Tablets are packed in a labeled…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Reese Pharmaceutical Company
FDA (openFDA food enforcement)
Reported Sep 21, 2016
T2Candida¿Cartridges; Part Number: 90-01794 (box of 12) and Part Number: 91-01534 (individual cartridge base). A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.T2 Biosystems Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aribex Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Geneva Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 14, 2016
The system provides the ability to transmit patient data files for storage, viewing and analysis at distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Sep 14, 2016
The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
IQF 1/4" Yellow Onion Dice, frozen, item numbers: 103364, 103381, and 104831, bulk cases, net wt. 45 lbs.; 11244CH…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Potato Company
8 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2016
TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2016
NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 17, 2016
lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one per carton. The lnvacare Precise Rx Pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Healthwise, Protein Chips, Barbecue Crunch, Net Weight 1.2 ounces (34 grams), Distributed by Nutritional Resources,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutritional Resources Inc.
FDA (openFDA food enforcement)
Reported Aug 10, 2016
SureStep Tray, with Add-a-Foley, COMPLETE CARE, Drainage Bag, and STATLOCK Stabilization The product is a urine…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2016
Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2016
RePlant¿ Angled Abutment Part Number 6050-52-60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Aug 10, 2016
Synergy Cranial S7. The software application is sent in CD format with an IFU, wrapped in plastic with a label for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2016
ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
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.