State

Utah product recalls

72,992 recalls have nationwide distribution and so reach Utah. 4,902 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,902
Critical: 524
Severe: 1,091
Most recent: 2026-09-16

Of the 4,902 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 4,902 recalls whose distribution notice names Utah specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7301–7325 of 77894

SevereFDA (Devices)·Z-1497-2025·2025-04-09
Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V216000·2025-04-09
McLaren brake lines may be routed to the wrong side
McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.
Product
MCLAREN — MCLAREN 600LT, GTS, 720S SPIDER, ARTURA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1494-2025·2025-04-09
Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
Product
Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2025·2025-04-09
Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect
Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.
Product
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2025·2025-04-09
Nasopore FD nasal dressing recalled for potential sterile barrier breach
Stryker Corporation is recalling 182,344 units of Nasopore FD nasal dressing nationwide due to potentially breached sterile seals that may allow product contamination.
Product
Nasopore FD fragmentable nasal dressing, Catalog Numbers 5400-020-108 and 5400-020-108ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0308-2025·2025-04-09
Prescription Duloxetine Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine 30 mg capsules distributed nationwide due to a nitrosamine impurity above acceptable limits. Consumers should consult their doctor about their medication.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0306-2025·2025-04-09
Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications
Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0685-2025·2025-04-09
SeaBear Clam Chowder Recalled for Potential Botulinum Contamination
SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.
Product
SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25E025000·2025-04-09
Hiab Recalls Waltco ZS-MK2 Lift Gates Due to Pin Seizure Risk
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2025·2025-04-09
Hemopore nasal wound dressing packaging seal defect may compromise sterility
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Product
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2025·2025-04-09
Nasopore Standard Nasal Dressing Recalled Due to Sterility Seal Defects
Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.
Product
Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1489-2025·2025-04-09
Stryker Spine Monterey AL Implant Inserter Gold Unlock Button Separation Recall
Stryker Spine has recalled 56 units of the Monterey AL Implant Inserter due to potential separation of the gold unlock button. This could impair the device's function during surgical implant placement.
Product
Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1506-2025·2025-04-09
Medtronic A820 myPTM Infusion Pump Software Shows Delayed Patient Response
Medtronic is recalling the A820 myPTM Software Application used with SynchroMed infusion pumps because the app is taking longer than expected to respond to patient interactions. Approximately 4365 units are affected worldwide.
Product
A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1488-2025·2025-04-09
Stryker Monterey AL Implant Inserter Gold Button Detachment Risk
Stryker Spine is recalling Monterey AL Implant Inserters due to a potential defect where the gold unlock button may separate from the device, compromising its function during spinal surgery.
Product
Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1474-2025·2025-04-09
Nasopore nasal dressing recall: compromised sterile barrier seals
Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.
Product
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0682-2025·2025-04-09
Lean Cuisine Butternut Squash Ravioli Recalled for Potential Foreign Material
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Product
Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1509-2025·2025-04-09
BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Product
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Category
Medical Device
Distribution
35 states
HighNHTSA·25V226000·2025-04-09
Audi Q6 rearview camera image may be delayed or deactivated
Volkswagen is recalling certain 2025 Audi Q6 and SQ6 vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse, failing FMVSS 111.
Product
AUDI — AUDI SQ6 SPORTBACK E-TRON, Q6 E-TRON
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2025·2025-04-09
Phoroptor VRx Digital Refraction System Recalled for Detachable Head
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25C005000·2025-04-09
Chicco Recalls MyFit Zip Air Harness and Booster Child Seats
Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2025·2025-04-09
Clinical Chemistry Analyzer Recalled for Software Defect in Test Result Calculation
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to a software defect that prevents calculated test results from being recalculated when constituent tests are rerun, potentially delaying patient result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0681-2025·2025-04-09
Lean Cuisine Lemon Garlic Shrimp Stir Fry Recalled Due to Foreign Material
Nestle-USA recalls Lean Cuisine Lemon Garlic Shrimp Stir Fry (10 oz) due to potential wood-like foreign material. Approximately 7,212 cases distributed across 37 states; check Batch Number 4214595511 (Best By September 2025).
Product
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Food)·F-0684-2025·2025-04-09
SeaBear Salmon Chowder Recalled for Potential Seal Failure and Botulinum Risk
SeaBear Smokedhouse Salmon Chowder is recalled due to potential seal failure that could allow Clostridium botulinum contamination. The recall affects 11,152 pouches distributed nationwide.
Product
SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2025·2025-04-09
Otopore Cylinder Wound Dressing Recalled for Potential Sterility Seal Defect
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing due to potential bubbles in blister seals that may breach the sterile barrier. Affected units were distributed nationwide.
Product
Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2025·2025-04-09
Ethicon Surgical Sutures Recalled Due to Silicone Curing Manufacturing Defect
Ethicon Endo Surgery recalls approximately 1,080 surgical sutures due to silicone curing issues identified during manufacturing. The defect may affect suture performance during surgical use.
Product
PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1
Category
Medical Device
Distribution
Distributed nationwide