State

Wyoming product recalls

72,992 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total: 3,219
Critical: 762
Severe: 543
Most recent: 2026-09-02

Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.

Which agencies issued them

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6301–6325 of 76211

SevereFDA (Devices)·Z-1972-2025·2025-06-18
BD Texium Closed System Drug Transfer Devices May Leak at Connector
BD Texium closed system drug transfer devices in multiple sizes may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, exposure to hazardous drugs, and underdosing.
Product
BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0464-2025·2025-06-18
MALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients
MALEXTRA Recharge with Extra dietary supplement is being recalled nationwide because laboratory testing found undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil in the product.
Product
MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0466-2025·2025-06-18
Dietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
ULTRA ARMOR dietary supplement, distributed by Health Fixer, is recalled nationwide because it contains undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1915-2025·2025-06-18
Covidien Newport HT70 and HT70Plus Ventilators Capacitor Failure Recall
Covidien is recalling Newport HT70 and HT70Plus ventilators due to capacitor failures that may cause the device to shut down unexpectedly or fail to alarm, risking respiratory failure and oxygen deprivation in patients.
Product
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1953-2025·2025-06-18
Tecfen Medical 20G MVR Sideport Knife ophthalmic sterility recall
Tecfen Medical is recalling its 20G (1.2mm) MVR Sideport Knife Straight (Model QKN2312) ophthalmic knives due to sterility assurance concerns. The recall affects 38 units distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 20G (1.2mm) MVR Sideport Knife Straight Model/Catalog Number: QKN2312 Software Version: No software Product Description: This is an ophthalmic knife (manual( that is to be sterile and packaged individually in Tyvek 1059B. MVR sideport
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25351·2025-06-18
MaxKare Electric Blankets Recalled for Burn and Fire Hazards
MaxKare electric blankets (model HB18A) sold on Walmart.com can overheat and catch fire, posing burn hazards. Yumo has received 34 reports of overheating, including 3 burn injuries and 2 fires.
Product
MaxKare Electric Blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0488-2025·2025-06-18
Sulfamethoxazole and Trimethoprim Tablets Recalled for Microbial Contamination
Amneal Pharmaceuticals is recalling Sulfamethoxazole and Trimethoprim Tablets (400 mg/80 mg) nationwide due to microbial contamination that may cause black spots on tablets. The contamination affects non-sterile products distributed across the USA.
Product
SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0463-2025·2025-06-18
Dietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients
Male Ultra dietary supplement, distributed nationwide in 3,000 boxes, has been recalled because laboratory testing found it contains undeclared pharmaceutical ingredients: propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0465-2025·2025-06-18
Dietary Supplement Electro Buzz Recalled for Undeclared Active Pharmaceutical Ingredients
SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement (lot KT-1ST-43-01-07/2024, expiring 10/15/2026) distributed nationwide. Laboratory testing found undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
Product
ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0459-2025·2025-06-18
Celecoxib Capsules 200 mg recalled for foreign tablets inside bottles
Alembic Pharmaceuticals is recalling Celecoxib 200 mg capsules after a customer found a Tadalafil 5 mg tablet inside a sealed 500-count bottle. The contamination was discovered through a customer complaint.
Product
Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1952-2025·2025-06-18
Tecfen Medical 2.8mm Slit Knife Angled Sterility Assurance Recall
Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife, Angled Model/Catalog Number: QKN2808 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V413000·2025-06-18
Mazda CX-50 airbag module software may cause improper deployment
Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.
Product
MAZDA — MAZDA CX-50 HYBRID, CX-50
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1935-2025·2025-06-18
Philips Intera Achieva 1.5T Pulsar MRI Systems Gradient Coil Fire Risk
Philips is recalling certain Intera Achieva 1.5T Pulsar MRI systems due to a potential component failure in the gradient coil that could generate smoke and/or fire, risking patient and operator injury or death.
Product
Intera Achieva 1.5T Pulsar; Product Number: 781171;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1934-2025·2025-06-18
Philips Intera 1.5T MRI Systems Gradient Coil Fire Risk Recall
Philips is recalling Intera 1.5T Omni/Stellar MRI systems due to a gradient coil component failure that can produce smoke and fire, risking patient and operator injury or death.
Product
Intera 1.5T Omni/Stellar; Product Number: 781104;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1921-2025·2025-06-18
SOLTIVE Premium SuperPulsed Laser System surgical instrument thermal incident
Olympus is recalling the SOLTIVE Premium SuperPulsed Laser System due to risk of thermal incidents including smoke, sparks, burning, or flames during clinical use caused by fiber fracturing.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1929-2025·2025-06-18
Philips Intera 1.5T Achieva IT Nova MRI System Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Achieva IT Nova MRI system due to a gradient coil component that may overheat and produce smoke or fire, posing risks of inhalation injury, burns, or death.
Product
Intera 1.5T Achieva IT Nova Product Number: 781175
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1936-2025·2025-06-18
Philips SmartPath to dStream 1.5T MRI Gradient Coil Fire Risk
Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.
Product
SmartPath to dStream for 1.5T¿; Product Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1868-2025·2025-06-18
Z-800WF Infusion System software verification defect recall
Zyno Medical LLC is recalling 613 units of the Z-800WF Infusion System because unreleased software versions were installed on distributed devices without verification or validation.
Product
Z-800WF Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25342·2025-06-18
AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards
AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.
Product
4 Liter/6 Can Minifridges
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1930-2025·2025-06-18
Philips Intera 1.5T Achieva Nova MRI Systems Gradient Coil Fire Risk
Philips is recalling certain Intera 1.5T Achieva Nova MRI systems due to a gradient coil component that can overheat, potentially causing smoke or fire with risk of burns, smoke inhalation, or asphyxia.
Product
Intera 1.5T Achieva Nova Product Number: 781172;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1928-2025·2025-06-18
Philips Achieva XR MRI systems recall for fire hazard
Philips Achieva XR MRI systems may have a gradient coil component failure that can generate heat, smoke, and fire. The risk to patients and operators includes inhalation of smoke, burns, and asphyxia.
Product
Achieva XR Product Numbers: (1) 781153, (2) 781253;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1969-2025·2025-06-18
Azurion R1.x and R2.x X-ray systems software communication issue
Philips Medical Systems has recalled Azurion R1.x and R2.x X-ray systems worldwide due to a software issue that can cause loss of imaging functionality and delay treatment, potentially resulting in serious harm or death in patients undergoing urgent or complex interventions.
Product
Azurion R1.x and R2.x systems; Model Numbers: (1) 722063, (2) 722064, (3) 722067, (4) 722068, (5) 722078, (6) 722079, (7) 722221, (8) 722222, (9) 722223, (10) 722224, (11) 722225, (12) 722226, (13) 722227, (14) 722228, (15) 722280, (16) 722281, (17) 722282; Software Version: Al
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0935-2025·2025-06-18
Instant Milk Tea Brown Sugar Powder recalled for undeclared milk allergen
R&M Refresher brand Instant Milk Tea Brown Sugar Flavor is recalled because the ingredients contain milk (Whey Powder, Sodium Caseinate) but the label does not declare milk as an allergen.
Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent ASIN #B0D728CZWS 3-pack ASIN #B0D72FQVDR Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Dis
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0934-2025·2025-06-18
Instant Milk Tea Powder lacks milk allergen declaration
R&M Trading LLC is recalling Instant Milk Tea Original Flavor because the label does not declare milk, despite containing whey powder and sodium caseinate, which are milk-derived ingredients.
Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71YHZX4 3-pack ASIN #B0D72BLQRW Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1920-2025·2025-06-18
SOLTIVE Pro SuperPulsed Laser System surgical instrument thermal incident
Olympus Corporation of the Americas is recalling the SOLTIVE Pro SuperPulsed Laser System due to risk of unexpected smoke, sparks, burning, or unsteady flames caused by fiber fracturing during clinical use.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Number: TFL-SLS, TFL-SLS-JA (Japan only); Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and flexibility to ureteroscopy,
Category
Medical Device
Distribution
Distributed nationwide