State

Utah product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41001–41025 of 78733

HighFDA (Devices)·Z-2102-2018·2018-06-13
GE Healthcare Recalls Centricity Universal Viewer for Missing Image Series
GE Healthcare is recalling 252 units of the Centricity Universal Viewer because image series may be missing from exams without a user warning.
Product
Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed, communicated, processed and displayed within the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2097-2018·2018-06-13
Tosoh ST-AIA PACK IGE II Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK IGE II allergy assays because Asfotase Alfa (Strensiq) can cause inaccurate test results.
Product
ST-AIA PACK IGE II; Part Number: 025295 Assay, Allergy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2077-2018·2018-06-13
Tosoh AIA-PACK TSH 3rd Generation Assay Recalled Due to Interference
Tosoh Bioscience Inc is recalling AIA-PACK TSH 3rd Generation assays because Asfotase Alfa interferes with the tests, potentially causing inaccurate results.
Product
AIA-PACK TSH 3rd Generation; Part Number: 020294 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2072-2018·2018-06-13
Tosoh Myoglobin Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK Myoglobin assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK Myoglobin; Part Number: 025297 Assay, Cardiac Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1884-2018·2018-06-13
Santajoy Laser Projectors Recalled for Exceeding Federal Radiation Standards
Santajoy Ornament & Giftware Co. is recalling E-Z Illuminations laser projectors because they may emit radiation exceeding federal standards for Class IIIa products.
Product
Santajoy Ornament & Giftware Co., Ltd E-Z Illuminations Northern Lights E-Z Illuminations Galaxy Laser projectors that emit various colors and light patterns for entertainment and decorative purposes.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2018·2018-06-13
Tosoh ST-AIA PACK IRI Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK IRI assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK IRI; Part Number: 025260 Assay, Diabetes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2051-2018·2018-06-13
Mako Surgical Recalls Restoris MCK Onlay Insert Extractor Due to Hinge Pin Risk
Mako Surgical Corporation is recalling 575 units of the Restoris MCK Onlay Insert Extractor because the hinge pin may disassociate.
Product
Restoris MCK Onlay Insert Extractor.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-2066-2018·2018-06-13
Tosoh ST-AIA PACK CEA Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK CEA assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK CEA; Part Number: 025254 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2081-2018·2018-06-13
Tosoh Thyroid Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK FT4 assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK FT4; Part Number: 025268 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2055-2018·2018-06-13
Becton Dickinson Recalls BD Vacutainer Plus SST Tubes Due to Stopper Defect
Becton Dickinson is recalling BD Vacutainer Plus SST tubes because the stoppers may pull out of the tubes.
Product
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1540-2018·2018-06-13
Heritage Shortbread Lemon Infused Recalled for Missing Wheat Labeling
Heritage Shortbread is recalling Lemon Infused shortbread because the label failed to list wheat as an ingredient.
Product
Heritage Shortbreaad Lemon Infused Ingredients: Enriched flour, pasteurized cream(milk),sugar, salt, pure crystallized ginger, organic ground ginger Mfg. by Heritage Shortbread, Inc. Hilton Head Island, SC 09926
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-2086-2018·2018-06-13
Tosoh FSH Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc. is recalling ST-AIA PACK FSH assays because the drug Asfotase Alfa (Strensiq) can cause inaccurate test results.
Product
ST-AIA PACK FSH; Part Number: 025265 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2078-2018·2018-06-13
Tosoh Thyroid Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK TT3 thyroid assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK TT3; Part Number: 025282 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2056-2018·2018-06-13
BD Vacutainer Plus SST Tubes Recalled for Stopper Defect
Becton Dickinson is recalling BD Vacutainer Plus SST tubes because the stoppers may pull out of the tube.
Product
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0841-2018·2018-06-13
Apotex Recalls Fluticasone Propionate Nasal Spray Due to Glass Particles
Apotex Inc. is recalling Fluticasone Propionate Nasal Spray because glass particles were found in the product. Consumers should stop using the affected lot.
Product
FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2018·2018-06-13
Tosoh ST-AIA PACK hsE2 Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK hsE2 assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK hsE2; Part Number: 025225 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2018·2018-06-13
Tosoh ST-AIA PACK AFP Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK AFP assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK AFP; Part Number: 025252 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2088-2018·2018-06-13
Tosoh Estradiol Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK Estradiol assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK Estradiol; Part Number: 025274 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2069-2018·2018-06-13
Tosoh ST-AIA CA 19-9 Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK CA 19-9 assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK CA 19-9; Part Number: 025271 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2095-2018·2018-06-13
Tosoh ST-AIA PACK HGH Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK HGH assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK HGH; Part Number: 025266 Assay, Metabolic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2090-2018·2018-06-13
Tosoh ST-AIA PACK LH II Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK LH II assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK LH II; Part Number: 025296 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2093-2018·2018-06-13
Tosoh ST-AIA PACK Testosterone Assay Recalled Due to Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK Testosterone assays because Asfotase Alfa interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK Testosterone; Part Number: 025204 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2075-2018·2018-06-13
Tosoh ST-AIA C-Peptide II Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK C-Peptide II assays because the drug Asfotase Alfa can cause inaccurate test results.
Product
ST-AIA PACK C-Peptide II; Part Number: 025283 Assay, Diabetes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1545-2018·2018-06-13
Dean Foods Recalls Baskin Robbins Mint Chocolate Chip Ice Cream
Dean Foods is recalling Baskin Robbins Mint Chocolate Chip ice cream because it may contain unlabeled coconut, a major food allergen.
Product
Baskin Robbins Mint Chocolate Chip
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2111-2018·2018-06-13
CareFusion Recalls Alaris Extension Sets Due to Incorrect Tubing
CareFusion 303, Inc. is recalling Alaris Extension Sets with microbore tubing because manufacturing errors resulted in incorrect priming volumes.
Product
Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV…
Category
Medical Device
Distribution
10 states