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.
2,918 stored notices name Utah, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Utah too — those are in the archive.
Reported May 1, 2013
AU5800 Clinical Chemistry Analyzer The Beckman Coulter AU5800 Clinical Chemistry Analyzer is an automated chemistry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Canned mushrooms, #10 cans (Brites, not labeled)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.L. K. Bowman, Incorporated
FDA (openFDA food enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Menz Club, LLC
FDA (openFDA drug enforcement)
Reported Apr 24, 2013
Vitrea CT Multi-Chamber Cardiac Functional Analysis application on Vitrea version 5.2 (Vitrea Enterprise Suite 1.3 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Images, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
MUSCLEPHARM brand COMBAT POWDER (R), COOKIES 'N' CREAM, NATURAL AND ARTIFICAL FLAVORS, HYBRID SERIES DIETARY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.F.H.G Corporation dba Integrity Nutraceuticals
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 17, 2013
LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lighthouse For The Blind
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2013
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Chapter, Inc.
FDA (openFDA food enforcement)
Reported Apr 17, 2013
Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Flexible Grip which is part of the Synthes Universal Nail System. Indicated for the conventional (non-locking)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermo Fisher Scientific (Asheville) LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2013
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Torrent" irrigation tubing. Product Usage: The Torrent irrigation system (tubing and accessories to accommodate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Animas Corporation
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon Catheter. The Arrow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0 ml, 13 X 75 mm STERILE REF 364953. Becton…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir, Catalog number 05232732001. Used with the cobas¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
ARCHITECT HBsAg Qualitative Assay, List Number 4P53 and ARCHITECT HBsAg Qualitative Confirmatory Assay, List Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Miravalle brand "Pan Rallado Sazonado", 8 oz. Seasoned bread crumbs. Also packaged in 12 pack. Product labeling reads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Miravalle Food, Inc.
FDA (openFDA food enforcement)
Reported Apr 3, 2013
Intraosseous Fixation System (IFS) 1.7 mm, 2.0 mm & 2.5 mm Cannulated Drill Bit. Intended to stabilize and aid in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Opalescence Treswhite Supreme Peach Patient Kit
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ultradent Products, Inc.
FDA (openFDA food 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.