State

Utah product recalls

73,584 recalls have nationwide distribution and so reach Utah. 4,909 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,909
Critical: 524
Severe: 1,349
Most recent: 2026-10-14

Of the 4,909 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 1,349 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,909 recalls whose distribution notice names Utah specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

226–250 of 78493

CriticalFDA (Food)·H-1405-2026·2026-10-07
Todd's Seeds Broccoli & Friends Sprouting Seed Mix Recalled for Contamination
Todd's Seeds LLC is recalling Broccoli & Friends Sprouting Seed Mix because it contains alfalfa seed that may be contaminated with E. coli and/or Salmonella.
Product
Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa, Radish, Clover, packaged in 1 oz. sample packets and heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., 2.5 lb., and 5 lb.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3276-2026·2026-10-07
Volcano Corp Recalls Philips IntraSight Plus Systems Due to Data Error
Volcano Corp is recalling 19 Philips IntraSight Plus systems because software may incorrectly associate patient image data with the wrong medical record.
Product
Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3227-2026·2026-10-07
Medline Homecare Bed Hand Pendants Recalled for Fire Hazard
Medline is recalling specific homecare bed hand pendants because the pendant or wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire.
Product
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/ MDR107003E MDR530094 PENDANT, W/ 9V BATTERY BACKUP, F/ 2E BED MDR540094 PENDANT, W/ 9V BATTERY BACKUP, F/ 3E BED
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3328-2026·2026-10-07
Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk
Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers due to a risk of blood-to-glycol leaks during cardiopulmonary bypass procedures.
Product
Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 Model/Catalog Number: HX55W-S0 Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V659000·2026-10-07
Toyota Recalls 2026 RAV4 Plug-In Hybrids for Powertrain Shutdown Risk
Toyota is recalling 30,978 2026 RAV4 Plug-In Hybrid vehicles because a software error may cause the hybrid system to reduce power or shut down at higher speeds, increasing crash risk.
Product
TOYOTA — TOYOTA RAV4 PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V660000·2026-10-07
Freightliner and FCCC Trucks Recalled for Fuel Hose Separation Risk
Daimler Trucks North America is recalling certain Freightliner and FCCC trucks because fuel hoses may separate, causing leaks, engine stalls, and fire risks.
Product
FCCC — 2025 FCCC XCS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3327-2026·2026-10-07
Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk
Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers because a defect may cause blood to leak into the glycol heat transfer fluid.
Product
Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog Number: HX55V-S0W Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3228-2026·2026-10-07
Medline Homecare Beds Recalled for Fire Hazard in Hand Control Pendant
Medline Industries is recalling Basic and Medlite Homecare Beds due to a potential fire hazard involving the hand control pendant and wiring.
Product
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3252-2026·2026-10-07
Draeger VentStar Resus Neo Neonatal Breathing Circuit Recall
Draeger is recalling VentStar Resus Neo neonatal breathing circuits due to potential hose cracks that could cause leakage or disconnection.
Product
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a resuscitation module.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V658000·2026-10-07
BMW Recalls 2021-2024 R 18 Motorcycles for Fire Risk
BMW is recalling 2021-2024 R 18 motorcycles with optional reverse gear because a deteriorating seal may allow moisture to enter the control unit, causing overheating and increasing the risk of a fire.
Product
BMW — BMW R 18
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3331-2026·2026-10-07
Penumbra RED 62 Reperfusion Catheter Recalled for Fracture Risk
Penumbra Inc. is recalling 43 RED 62 Reperfusion Catheters due to manufacturing issues that may cause the catheters to fracture.
Product
Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter) Model/Catalog Number: THNDRRED62SKIT Software Version: N/A Product Description: Product common name: Percutaneous catheter A complete product description…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0876-2026·2026-10-07
Par Health Recalls Buprenorphine Hydrochloride Injection Due to Crystallization
Par Health USA is voluntarily recalling 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. The FDA classifies this as a Class II recall.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3294-2026·2026-10-07
FDA Recalls Medical Kits with Contaminated Pericare Wipes
American Contract Systems Inc. is recalling 1,804 medical kits containing BD CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989 Model No. MHAH55AM LAVH-LAP COLON Model No. SPLL54U VAG HYST PACK Model No. SPVH62P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3302-2026·2026-10-07
Heraeus Medical Recalls PALACOS R+G pro Bone Cement Due to Leakage Risk
Heraeus Medical GmbH is recalling PALACOS R+G pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall affects 59,660 units distributed worldwide.
Product
PALACOS R+G pro 40; PALACOS R+G pro 80. Model/Catalog Number: 5081288; 5081289. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3293-2026·2026-10-07
Recall of Medical Convenience Kits with Contaminated Pericare Wipes
American Contract Systems Inc. is recalling 1,804 medical convenience kits containing potentially contaminated perineal care wipes. The contamination may cause skin irritation or increase infection risk.
Product
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays CARDIAC HEART BUNDLE NS Model No. LMCH99P OPEN HEART 2 RCH¿ 0248495 Model No. RCOH62C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3324-2026·2026-10-07
Percussionaire Travel Air and Phasitron 5 Recall for Anesthetic Warning
Percussionaire Corporation is recalling Travel Air and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Product
Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3296-2026·2026-10-07
Cardinal Health Recalls Presource Packs Due to Potential Handpiece Leakage
Cardinal Health 200, LLC is recalling 344 Presource Packs containing Stryker tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Product
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT,GU DAVINCI , Catalog Number: PGVMDVBWU; 2) KIT,GU DAVINCI , Catalog Number: PGVMDVBWV; 3) KIT,GU DAVINCI , Catalog Number: PGVMDVB26; 4) KIT,GU DAVINCI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3301-2026·2026-10-07
Heraeus Medical Recalls PALACOS R pro Bone Cement Due to Leakage Risk
Heraeus Medical is recalling PALACOS R pro 40 and 80 bone cement because of a potential for monomer liquid leakage. The recall affects 33,727 units distributed worldwide.
Product
PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3291-2026·2026-10-07
FDA Recalls Opportunity Pro Nitrile Gloves Due to Manufacturing Defects
American Nitrile Operations LLC is recalling 17,481,000 Opportunity Pro nitrile gloves nationwide due to defects like tears and debris that may expose users to pathogens or chemicals.
Product
Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800, 72-50801,72-50802,72-50803,72-50804 Product Description: Blue Nitrile patient examination glove
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3295-2026·2026-10-07
Cardinal Health Recalls Stryker StrykeFlow PS and AHTO Tube Set Kits
Cardinal Health is recalling 3,677 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Product
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2) KIT, LAP CHOLE , Catalog Number: PGCGLCBAD; 3) KIT, LAP CHOLE , Catalog Number: PGCGLCBAE; 4) KIT, LAP CHOLE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3304-2026·2026-10-07
Heraeus Medical Recalls PALACOS MV Pro Bone Cement Due to Leakage Risk
Heraeus Medical is recalling PALACOS MV pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall covers all lot numbers distributed worldwide.
Product
PALACOS MV pro 40; PALACOS MV pro 80. Model/Catalog Number: 5150633; 5150635. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3277-2026·2026-10-07
United Imaging uCT 530 CT Systems Recalled for Software Visibility Issue
Shanghai United Imaging Healthcare is recalling four uCT 530 CT systems due to a software defect that may hide patient images, potentially requiring rescans.
Product
Computed Tomography X-ray System, Model: uCT 530 with software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3275-2026·2026-10-07
Bard EnCor EnCompass Breast Biopsy System Software Recall
Bard Peripheral Vascular Inc is recalling 99 EnCor EnCompass Breast Biopsy and Tissue Removal Systems due to software errors that may interrupt procedures.
Product
EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number: ENCPDRIVER) with software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3305-2026·2026-10-07
Embosphere Microspheres Recalled Due to Packaging Sterility Concerns
Merit Medical Systems is recalling Embosphere microspheres because packaging holes may compromise sterility, posing an infection risk.
Product
Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2 mL Syringe Sterile Steam, REF: S820GH/CAB; Embosphere 900-1200 micrometer 2 mL Syringe Sterile Steam, REF: S1020GH/C, S1020GH/EUA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3271-2026·2026-10-07
Alere hCG Pregnancy Test Cassettes Recalled for False Positive Results
Alere San Diego is recalling hCG rapid test cassettes because they may detect low hormone levels, leading to false positive pregnancy results.
Product
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part: FHC-A102/92210; Fisher Scientific Sure-Vue Serum/Urine¿hCG-STAT, Model/ Part: FHC-A202/23900531, FHC-A202/23900530; McKesson CONSULT Diagnostics hCG Urine…
Category
Medical Device
Distribution
Distributed nationwide