State

Utah product recalls

72,919 recalls have nationwide distribution and so reach Utah. 4,901 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,901
Critical: 524
Severe: 1,091
Most recent: 2026-09-09

Of the 4,901 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 1,091 (22%) are Severe.

Which agencies issued them

These figures cover only the 4,901 recalls whose distribution notice names Utah specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1551–1575 of 77820

HighFDA (Food)·H-0980-2026·2026-06-10
Albertsons banana nut muffins do not declare walnut allergen
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Product
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0958-2026·2026-06-10
Albertsons colossal Dubai cheesecake slice does not declare pistachio
Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.
Product
UPC 25216200000 Cheesecake Slice Colossal Dubai. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0554-2026·2026-06-10
Spectra lidocaine ampules recalled over lack of sterility assurance
Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0996-2026·2026-06-10
Imitation crab and shrimp sriracha salad does not declare pollock
Albertsons store-made Imitation Crab and Shrimp Salad Sriracha is being recalled because the contains statement does not declare pollock. 15 units are affected.
Product
UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0992-2026·2026-06-10
Albertsons elegant charcuterie tray does not declare pistachio allergen
Albertsons store-made Tray Charcuterie Elegant is being recalled because the contains statement does not declare pistachio. Eight units are affected.
Product
UPC 29138800000 TRAY CHARCUTERIE ELEGANT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0569-2026·2026-06-10
Family Wellness ultra strength antacid tablets contain metallic particles
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
Product
FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2026·2026-06-10
BD Pyxis MedBank Mini fingerprint scanner may overheat and burn
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2026·2026-06-10
Phothera 200 phototherapy calibration certificates had outputs reversed
Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.
Product
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2026·2026-06-10
Stapes prosthesis pistons carry an incorrect functional length on labeling
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Product
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1021-2026·2026-06-10
Albertsons grilled chicken salad does not declare almond allergen
Albertsons store-made Kitchen Salad Grilled Chicken is being recalled because the contains statement does not declare almond. 27 units are affected.
Product
UPC 27163100000 Kitchen SALAD GRILLED CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0558-2026·2026-06-10
Tums assorted fruit antacid tablets contain small metallic particles
Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.
Product
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2271-2026·2026-06-10
Covidien esophageal stethoscope temperature sensors lack FDA clearance
Covidien Mon-a-Therm Esophageal Stethoscopes with Temperature Sensor 400TM, REF 90042, are being recalled because the devices lack FDA clearance. 23,000 units are affected.
Product
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2267-2026·2026-06-10
B. Braun spinal epidural kits contain Mastisol with cracking tubing
B. Braun Lyndon B Johnson Hospital spinal epidural kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Product
Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1009-2026·2026-06-10
Albertsons Old Bay seasoned shrimp omits shrimp declaration
Albertsons store-made Shrimp P&D Old Bay Seasoned is being recalled because the contains statement does not declare shrimp. Five units are affected.
Product
UPC 23036500000 SHRIMP P&D OLD BAY SEASONED This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0599-2026·2026-06-10
Xyvona 3 mg levorphanol tablets recalled after proprietary name denial
Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Product
Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-058-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0957-2026·2026-06-10
Albertsons yellow fudge pecan cake omits pecan from contains statement
Albertsons store-made Cake Yellow Fudge Pecan half 8-inch is being recalled because the contains statement does not declare pecan.
Product
UPC 28848900000 Cake Yellow Fudge Pecan 1/2 8IN This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2273-2026·2026-06-10
Covidien 9 Fr Mon-a-Therm temperature probes lack FDA clearance
Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.
Product
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2269-2026·2026-06-10
B. Braun Shands kits contain Mastisol adhesive with cracking tubing
B. Braun CESK Shands Jacksonville kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
Product
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1069-2026·2026-06-10
Albertsons lemon pepper kosher salmon omits salmon declaration
Albertsons store-made Salmon Lemon Pepper Kosher is being recalled because the contains statement does not declare salmon.
Product
UPC 21919300000 SALMON LEMON PEPPER KOSHER PO SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0973-2026·2026-06-10
Albertsons almond raspberry croissants omit almond from contains statement
Albertsons store-made Almond Raspberry Filled Croissants, 4 count, are being recalled because the contains statement does not declare almond. 15 units are affected.
Product
UPC 25317100000 CROISSANTS ALMOND RASPBERRY FILLED 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1041-2026·2026-06-10
Albertsons coco and hazelnut pop dots omit hazelnut declaration
Albertsons store-made Pop Dots Coco & Hazelnut, 6 count, is being recalled because the contains statement does not declare hazelnut. 25 units are affected.
Product
UPC 25800800000 POP DOTS COCO & HAZELNUT 6CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0598-2026·2026-06-10
Xyvona levorphanol tablets recalled after FDA denied the proprietary name
Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Product
Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-762-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2283-2026·2026-06-10
HiRes Ultra 3D cochlear implants carry an incorrect expiration date
HiRes Ultra 3D CI HiFocus Mid Scala cochlear implants are being recalled due to an incorrect shelf-life expiration date. 36 units are affected.
Product
Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic Ear System is a cochlear implant designed to provide useful hearing to individuals
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2265-2026·2026-06-10
B. Braun spinal epidural catheters contain Mastisol with cracking tubing
B. Braun NES1725KFXL spinal epidural closed tip catheters are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack. 1,730 units affected.
Product
Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1053-2026·2026-06-10
Albertsons wild salmon feta spinach burger omits salmon declaration
Albertsons store-made Wild Salmon Feta Spinach Burger is being recalled because the contains statement does not declare salmon. One unit is affected.
Product
UPC 23258300000 BURGER WILD SALMON FETA SPINACH This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide