State

Utah product recalls

73,833 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,916
Critical: 524
Severe: 1,351
Most recent: 2026-11-04

Of the 4,916 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,351 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53351–53375 of 78749

SevereFDA (Food)·F-0768-2016·2016-03-23
Wilderness Family Naturals Coconut Curry Recalled for Milk Contamination
Wilderness Family Naturals is recalling specific Coconut Vegetable Curry over Quinoa products due to potential milk contamination.
Product
Morning Star Disaster Supplies Coconut Vegetable Curry over Quinoa, Net Wt 4.95 oz (115 g). UPC 853328-006069, Foil Bag Wilderness Family Naturals Quick Meal Coconut Vegetable Curry over Quinoa, Net Wt 4.95 oz (115 g). UPC 853328-006229, Foil Bag
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·16V168000·2016-03-23
Chrysler Recalls 2015-2016 Jeep and Dodge Vehicles for Brake Caliper Defect
Chrysler is recalling 21,183 2015-2016 Jeep Grand Cherokee and Dodge Durango vehicles because the left front brake caliper may crack, increasing stopping distance and crash risk.
Product
DODGE — DODGE, JEEP DURANGO, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0769-2016·2016-03-23
Wilderness Family Naturals Jamaican Beans and Rice Recalled for Milk Contamination
Wilderness Family Naturals is recalling specific lots of Jamaican Beans and Rice products due to potential milk contamination.
Product
Morning Star Disaster Supplies Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 853328-006076, Foil Bag Wilderness Family Naturals Quick Meal Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 898392-007987, Foil Bag
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0759-2016·2016-03-23
Wilderness Family Naturals Coconut Chia Pudding Mix Recalled for Milk Contamination
Wilderness Family Naturals is recalling Organic Coconut Chia Pudding Mix due to potential milk contamination. The product was distributed nationwide in the US and in Canada.
Product
Wilderness Family Naturals Coconut Chia Pudding Mix Organic, packaged in the following sizes: 1.1 lb Plastic Bag, UPC 898392-007789, and 13.2 lb. (12 plastic bags in a cardboard box) UPC 01002466
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0763-2016·2016-03-23
Wilderness Family Naturals Organic Coconut Milk Powder Recalled for Milk Contamination
Wilderness Family Naturals is recalling Organic Coconut Milk Powder and products containing it due to potential milk contamination.
Product
Wilderness Family Naturals Banana Blueberry Cereal Organic 8 oz.., Foil Bag UPC 898392-007833
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0762-2016·2016-03-23
Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination
Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.
Product
Wilderness Family Naturals Choco Maca Strawberry Cereal Organic 8 oz.., Foil Bag UPC 898392-007819
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0751-2016·2016-03-23
Casper's Sea Salt Caramel Pretzel Ice Cream Recalled for Allergen Mislabeling
Casper's Ice Cream is recalling Sea Salt Caramel Pretzel Ice Cream because it contains Caramel Cashew ice cream, presenting a potential allergen threat.
Product
Sea Salt Caramel Pretzel Ice Cream, Red Button Vintage Creamery, 56 fluid ounce, Paper Tub, 6 tubs per case, Distributed by Associated Foods, Inc. Utah; Manufactured by Caspers Ice Cream, Inc. Utah
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1185-2016·2016-03-23
Stryker Recalls 36 Non-Powered Stretchers Due to Hydraulic Jack Assembly Defect
Stryker is recalling 36 non-powered stretchers because hydraulic jack assemblies were manufactured with incorrect oil, increasing the risk of leaks or jack drift.
Product
Transport Stretcher, and Head and Neck Surgery Stretcher Non-powered stretcher
Category
Medical Device
Distribution
15 states
HighFDA (Devices)·Z-1148-2016·2016-03-23
Zimmer NexGen MIS Tibia Plate Recall for Sterility Concerns
Zimmer Manufacturing B.V. is recalling NexGen MIS Tibia Plates due to insufficient sealer calibration data, raising concerns about the sterility of the devices.
Product
Product 50 consists of all product under product code: JWH and same usage: Item no: 595002701 NEXGEN MIS TIBIA PLATE PR 595002702 NEXGEN MIS TIBIA PLATE PR 595003701 NEXGEN MIS TIBIA PLATE PR 595003702 NEXGEN MIS TIBIA PLATE PR 595003712 NEXGEN MIS TIBIA PLATE PR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1161-2016·2016-03-23
Zimmer Manufacturing Recalls Trilogy Acet Shells Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling 2,063 units of Trilogy Acet Shells used in total hip arthroplasty due to insufficient sealer calibration data.
Product
Product 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM O 620004220 TRILOGY ACET SHELL 42MM O 620004420 TRILOGY ACET SHELL 44MM O 620004620 TRILOGY ACET SHELL 46MM O 620004621 TRILOGY ACET SHELL 46MM O…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2016·2016-03-23
Zimmer Manufacturing Recalls Unipolar Femoral Heads Due to Sterility Concerns
Zimmer Manufacturing B.V. is recalling 2,239 unipolar femoral heads used in hip arthroplasty due to insufficient sealer calibration data, raising concerns about the sterility of the devices.
Product
Product 3 consists of all products under product code JDI, and same usage: Item no:781803800 12/14 UNIPOLAR FEMORAL HE 781804000 12/14 UNIPOLAR FEMORAL HE 781804100 12/14 UNIPOLAR FEMORAL HE 781804200 12/14 UNIPOLAR FEMORAL HE 781804300 12/14 UNIPOLAR FEMORAL HE 781804400…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1133-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Knee Fluted Rods Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 49 units of sterile I/B II Knee Fluted Rods due to insufficient sealer calibration data.
Product
Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1 for use in total knee arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V166000·2016-03-23
Bugatti Recalls Veyron Models Due to Corroding Underbody Aluminum Plates
Bugatti is recalling 2006-2013 Veyron models because underbody aluminum plates may corrode and detach, posing a road hazard to other vehicles.
Product
BUGATTI — BUGATTI VEYRON, VEYRON GRAND SPORT, VEYRON SUPER SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1100-2016·2016-03-23
Zimmer Manufacturing Recalls Hip Femoral Heads Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling 35,032 hip femoral heads due to insufficient sealer calibration data. The affected sterile products were packaged between August 2010 and April 2013.
Product
Product 2 consists of all products product code LPH, and same usage: 801802202 12/14 COCR FEMORAL HEAD 2 801802220 12/14 COCR FEMORAL HEAD 2 801802230 12/14 COCR FEMORAL HEAD 2 801802601 12/14 COCR FEMORAL HEAD 2 801802602 12/14 COCR FEMORAL HEAD 2 801802603 12/14 COCR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1126-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Femoral Hip Implant Components
Zimmer Manufacturing B.V. is recalling specific sterile femoral hip implant components due to insufficient sealer calibration data.
Product
Product 28 consists of all product under product code: JDI and same usage: Item no: 32902605000 FEMORAL HD 28MM MEDIUM 32902604000 FEMORAL HD 28MM SHORT 32902604035 FEMORAL HD 28MM SHT+ 3.5M For use in total or hemi hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1172-2016·2016-03-23
Roche Recalls Accu-Chek Inform II Base Units Due to Data Loss Risk
Roche is recalling Accu-Chek Inform II Base Units because they may lose data or mismatch patient records when connected to specific Data Management Systems.
Product
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II Blood Glucose Monitoring System is intended for testing outside the body (in vitro diagnostic use) and is intended for multiple-patient use in professional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1137-2016·2016-03-23
Zimmer Ion Implanted Femoral Stems Recalled for Sterility Concerns
Zimmer Manufacturing B.V. is recalling 17 ion implanted femoral stems used in hip arthroplasty due to insufficient sealer calibration data affecting sterility.
Product
Product 39 consists of all product under product code: JDI and same usage: Item no: 32902605800 ION IMPLANTED FEM 22MM LO 32902604900 ION IMPLANTED FEM 26MM ME 32902603900 ION IMPLANTED FEM 26MM SH For use in total or hemi hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1176-2016·2016-03-23
CHG Hospital Beds Recalls Spirit Select Beds Due to Alarm Defect
CHG Hospital Beds is recalling 1,892 Spirit Select beds because the bed exit alarm may fail to function, potentially delaying assistance after a patient fall.
Product
The Spirit TM Select bed is a Med-Surg bed intended to support and transport low to moderate acuity patients in the medical and/or surgical area of the hospital. The Spirit Select bed is also intended for use as a general purpose, variable height hospital bed for general care…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2016·2016-03-23
Cordis Avanti Catheter Sheath Introducer System Recalled for Incorrect Cannula Size
Cordis Corporation is recalling 1,985 units of the Avanti Catheter Sheath Introducer System because the cannula is smaller than intended.
Product
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator. A Catheter Sheath Introducer facilitates percutaneous entry of an intravascular device. A vessel dilator facilitates the percutaneous entry of the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2016·2016-03-23
Zimmer Free-Lock Tube and SCP Plate Recall for Sterility Concerns
Zimmer Manufacturing B.V. is recalling 285 units of Free-Lock Tube & SCP Plate devices due to insufficient sealer calibration data affecting sterility.
Product
Product 31 consists of all product under product code: KTT and same usage: Item no: 118113003 FREE-LOCK TUBE & SCP PLAT 118113502 FREE-LOCK TUBE & SCP PLAT 118113503 FREE-LOCK TUBE & SCP PLAT 118114002 FREE-LOCK TUBE & SCP PLAT 118114003 FREE-LOCK TUBE & SCP PLAT…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1182-2016·2016-03-23
McKesson Medical Imaging Software Recalled for Potential Image Display Errors
McKesson is recalling Horizon Medical Imaging and Radiology software due to a design deficiency that may cause incorrect patient images to be displayed.
Product
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products 12.0 and 12.1.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2016·2016-03-23
Zimmer NexGen Osteotomy Cortical Bone Screws Recalled for Sterility Concerns
Zimmer Manufacturing B.V. is recalling NexGen Osteotomy Cortical Bone Screws due to insufficient sealer calibration data, raising concerns about the sterility of the devices.
Product
Product 52 consists of product code: HWC and same usage: Item no: 525004530 NEXGEN OSTEOTOMY CORT BON 525004540 NEXGEN OSTEOTOMY CORT BON 525006545 NEXGEN OSTEOTOMY CORT BON 525006560 NEXGEN OSTEOTOMY CORT BON 525006565 NEXGEN OSTEOTOMY CORT BON for use in total knee…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1164-2016·2016-03-23
Zimmer Versys Advocate Hip Implants Recalled for Calibration Issues
Zimmer Manufacturing B.V. is recalling Versys Advocate hip implants due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERSYS ADVOCATE CEMENTED 785001220 VERSYS ADVOCATE CEMENTED 785001300 VERSYS ADVOCATE CEMENTED 785001320 VERSYS ADVOCATE CEMENTED 785001400…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1098-2016·2016-03-23
Deerfield Imaging Recalls Intraoperative MRI Systems Due to Venting Line Defect
Deerfield Imaging is recalling specific intraoperative MRI systems because emergency helium venting lines may not have been properly installed.
Product
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic resonance diagnostic device (MRDD).
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-1110-2016·2016-03-23
Zimmer Manufacturing Recalls 6 Degree COCR Femoral Heads for Sterility Concerns
Zimmer Manufacturing B.V. is recalling 209 units of 6 Degree COCR Femoral Heads due to insufficient sealer calibration data. The affected sterile products were distributed nationwide in the US.
Product
Product 12 consists of all product under product code JDI , and same usage: Item no: 902602935 6 DEGREE COCR FEM HEAD 28 902602835 6 DEGREE COCR FEM HEAD 28 902603235 6 DEGREE COCR FEM HEAD 32 902603335 6 DEGREE COCR FEM HEAD 32 902603600 6 DEGREE COCR FEM HEAD 36…
Category
Medical Device
Distribution
Distributed nationwide