Utah recalls
3512 federal recalls on file affecting Utah - 432 Utah-specific plus 3080 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2014-10-08USDAClass INationwideFirma De Minnesota Retira Del Mercado Productos De Carne De Res Y Aves Debido A Posible Contaminacion Con Listeria
Product Contamination
- 2014-09-25USDAClass IDo not eat Foster Farms frozen chicken breast strips
Product Contamination
- 2014-09-23USDAClass IDon't eat Applegate Naturals beef corn dogs
Processing Defect
- 2014-08-21USDAClass INationwideDo not eat APPA Fine Foods chicken caesar salad
Product Contamination
- 2014-08-12USDAClass IINationwideDon't eat Applegate Naturals chicken nuggets
Product Contamination
- 2014-08-09USDAClass IIINationwideCheck Oberto's chicken strips for swollen packages
Processing Defect
- 2014-08-06USDAClass INationwideDo not eat Cavanaugh Smoked Sausage
Misbranding, Unreported Allergens
- 2014-07-22USDAClass IINationwideDo not serve Sara Lee smoked sausage
Misbranding, Unreported Allergens
- 2014-07-12USDAClass ICheck freezer for recalled Foster Farms chicken
Product Contamination
- 2014-06-19USDAClass INationwideDo not eat Thai Kitchen Chicken Pad Thai
Misbranding, Unreported Allergens
- 2014-05-21USDAClass INationwideDo not eat recalled Wegmans or Sugar Lake Farms chicken strips
Misbranding, Unreported Allergens
- 2014-04-20USDAClass INationwideStop using Oscar Mayer Classic Wieners
Misbranding, Unreported Allergens
- 2014-04-19USDAClass INationwideDon't serve Sugar Lake Farms chicken breast products
Misbranding, Unreported Allergens
- 2014-04-02USDAClass INationwideDon't eat Backpackers Pantry fettuccini alfredo
Misbranding, Unreported Allergens
- 2014-04-01USDAClass IDon't eat AdvancePierre chicken breast fritters
Misbranding, Unreported Allergens
- 2014-03-26USDAPublic Health AlertNationwideDo not eat Nutriom egg products
Unfit for Human Consumption
- 2014-02-18USDAClass INationwideDo not eat Rancho Feeding Corporation beef
Produced Without Benefit of Inspection
- 2014-02-15USDAClass INationwideCheck OvaEasy egg products for Salmonella risk
Product Contamination
- 2014-02-11USDAClass IINationwideStop eating recalled beef jerky products from Utah
Misbranding, Unreported Allergens
- 2014-02-08USDAClass IDiscard Wyoming Authentic Products beef jerky
Processing Defect
- 2014-02-04USDAClass INationwideStop eating Healthy Choice chicken soup bowls
Misbranding, Unreported Allergens
- 2014-02-01USDAClass IINationwideCheck House of Smoke sausage and meat products
Misbranding, Unreported Allergens
- 2014-01-27USDAClass IINationwideUna Firma En Arkansas Retira Del Mercado Productos De Pollo Congelado Debido A Alérgenos No Identificados
Misbranding, Unreported Allergens
- 2014-01-19USDAClass IINationwideCheck your Velveeta mac and cheese for soy allergen
Misbranding, Unreported Allergens
- 2014-01-10USDAClass INationwideCheck institutional chicken products for recall
Product Contamination
- 2013-10-09FDA-DeviceCordisClass IINationwideCheck Cordis ADROIT 6F catheter lot numbers
Due to a labeling error related to the conversion of the inner diameter of the catheter from inches to millimeters. The English dimension is correct and is the primary dimension.
- 2013-10-09FDA-DeviceKing SystemsClass IINationwideCheck King LTS-D airway size labeling
On December 13, 2012, King Systems initiated a voluntary recall of one (1) case(s) (5) individual products) from one (1) lot [(IV1V3) 62 cases, 310 products]of King LTSD Oropharyngeal Airways because the package label indicated that the airway was a size 5 when in fact the airway in the package was a size 4. When King manufacturers a lot, all of the components are the same size, part number etc. I
- 2013-10-09FDA-DeviceMaquetClass IINationwideContact Maquet about Ultima OPCAB blade mislabeling
MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers OM-2003S & OM-2001D). Labeling for the 2 blade lots had been incorrectly applied. The standard blades from Lot #25052176 were incorrectly labeled as deep blades, and the 20 deep blades from Lot #25052200 were incorrectly labeled as standard blades.
- 2012-10-10FDA-DeviceBeckman CoulterClass IINationwideStop using Beckman Coulter RF reagent lots M012376, M101865
The recall was initiated because Beckman Coulter has confirmed customer reports of QC shifts, lot-to-lot variation, and an increase in the percent of patient samples recovering >20 IU/mL using the Lots# M012376 and M101865 of IMMAGE RF reagent. The lots identified for the RF reagent might produce false abnormal results.
- 2012-10-10FDA-DeviceBeckman CoulterClass IINationwideCOULTER PrepPlus, Part Number: 286600 Product Usage: The COULTER PrepPlus, is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.
The recall was initiated because Beckman Coulter has confirmed that the Coulter PrepPlus may experience intermittant reagent level sense failures where the instrument may not produce a warning that a reagent vial is low or out of reagent.
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