The Recall Desk

State

Wyoming product recalls

72,936 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.

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1776–1800 of 76155

  • SevereCPSC·26502·2026-05-21

    Portable Hook-On Chairs Recalled Due to Fall Hazard Risk

    PandaEar is recalling about 9,700 portable hook-on chairs sold online because the crotch restraints can be removed without tools, allowing infants to fall through openings. No injuries have been reported.

    Product
    Portable Hook-On Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26501·2026-05-21

    Sierra 125U Youth All-Terrain Vehicles Recalled for Crash and Burn Hazards

    Lil Pick Up Inc. has recalled about 700 Sierra 125U Youth ATVs sold from October 2025 through April 2026 due to defects that violate federal safety standards and pose risks of serious injury or death, including suspension failures, faulty reverse lights, failing brakes, and hot surfaces.

    Product
    Sierra 125U Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26504·2026-05-21

    Bethlehem Lights 10-inch Illuminated Ribbon Spheres Recalled for Fire Hazard

    Bethlehem Lights 10-inch Illuminated Ribbon Spheres are recalled because the LED lights can overheat and spark, posing a risk of serious injury or death from fire. About 2,000 units sold online through QVC from July 2024 to April 2026 are affected.

    Product
    Bethlehem Lights 10-inch Illuminated Ribbon Spheres
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V329000·2026-05-21

    GM Recalls Cadillac Vehicles Due to Front Driver Air Bag Inflator Rupture Risk

    General Motors is recalling specific 2015-2016 Cadillac models because the front-driver air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    CADILLAC — CADILLAC ESCALADE ESV, SRX, ATS, CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26503·2026-05-21

    WSDZ Light-up Shot Glasses Recalled Due to Button Battery Ingestion Risk

    ABC Trading is recalling WSDZ Light-up Shot Glasses because the button cell batteries can be easily accessed by children, creating an ingestion hazard that can cause serious internal injuries or death. No injuries have been reported.

    Product
    WSDZ Light-up Shot Glasses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V325000·2026-05-21

    GM Recalls 2018-2019 Silverado and Sierra Trucks for Air Bag Defect

    General Motors is recalling 2018-2019 Chevrolet Silverado and GMC Sierra trucks because roof rail air bag inflators may rupture, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SILVERADO 2500, SILVERADO 3500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V332000·2026-05-21

    Honda and Acura vehicles recalled for faulty passenger seat weight sensor

    Honda and Acura are recalling multiple 2016–2026 model-year vehicles because the front passenger seat weight sensor may crack and short circuit, causing unintended airbag deployment during a crash.

    Product
    HONDA — HONDA, ACURA INSIGHT, MDX, ODYSSEY, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V326000·2026-05-21

    2026 Jeep Grand Wagoneer Recalled for Rearview Camera Wiring Defect

    Chrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles because a wiring issue may prevent the rearview camera image from displaying, increasing crash risk.

    Product
    JEEP — JEEP GRAND WAGONEER L, GRAND WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V327000·2026-05-21

    Chrysler and Ram rearview cameras may fail to display an image

    Chrysler is recalling certain Pacifica, Ram 1500, Ram 2500 and Jeep Wrangler vehicles because contamination or improper programming may stop the rearview camera image displaying.

    Product
    CHRYSLER — CHRYSLER, JEEP, RAM PACIFICA, WRANGLER, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V328000·2026-05-21

    2023–2025 Jeep Grand Cherokee L vehicles recalled for air bag software defect

    Chrysler is recalling certain 2022–2026 Jeep Grand Cherokee and 2023–2025 Jeep Grand Cherokee L vehicles due to a software error that may delay side air bag deployment during a crash. The defect increases injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26497·2026-05-21

    Children's Toys with Accessible Button Batteries Recalled for Ingestion Risk

    ABC Trading recalls toy headbands and electronic pet cages because button cell batteries are easily accessible to children, posing a risk of serious injury or death if swallowed. About 84,700 units sold nationwide from November 2022 through October 2025 are affected.

    Product
    Toy Headbands, Electronic Pet Cage-Dinosaur Tribes, My Pet Bird Cute Bird Tribes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V331000·2026-05-21

    2025-2026 Nissan Kicks combination meter software display defect

    Nissan is recalling 2025-2026 Kicks vehicles for a software error that may cause the combination meter display to go partially or fully blank, preventing visibility of critical safety information like vehicle speed and warning lights.

    Product
    NISSAN — NISSAN KICKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26499·2026-05-21

    Orb Funkee Squeeze Toys Recalled Due to Asbestos Exposure Risk

    The Orb Factory is recalling approximately 121,340 Orb Funkee squeeze toys (model 17451 and 41929) because the sand filling may contain fibrous tremolite asbestos. No illnesses have been reported, but inhalation of the asbestos fibers poses a serious health risk.

    Product
    Orb Funkee Squeeze Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26498·2026-05-21

    HomeProGym Resistance Bands Recalled Due to Impact Hazard

    HomeProGym is recalling certain purple 60-pound and gray 70-pound resistance bands because they can forcefully separate from the handle during use, posing a risk of serious injury. Five reports of separation have been received with no injuries reported.

    Product
    HomeProGym Resistance Bands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2159-2026·2026-05-20

    NextStep Hemodialysis Catheters with Defective Sheath Introducer

    Arrow International is recalling NextStep Antegrade and Retrograde Hemodialysis Catheters worldwide because an included 16F dual-valved splittable sheath introducer may not split as intended, potentially causing pain, bleeding, hematoma, and tissue injury.

    Product
    NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272-SFX, CS-15312-SFX, CS-15422-SFX, CS-15502-SFX; NextStep Antegrade Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15192-SFXM, CS-1523
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2138-2026·2026-05-20

    Namic Angiographic Manifold Recalled for Particulate Contamination

    Medline Industries is recalling approximately 7,075 units of the Namic Angiographic Manifold (SKU 64038200) due to particulate found in the fluid path. The manifold is used in cardiopulmonary bypass procedures and is distributed across the US and internationally.

    Product
    Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0525-2026·2026-05-20

    Oasis Tears PF Lubricant Eye Drops Recalled for Sterility Assurance

    Oasis Medical, Inc. is recalling Oasis Tears PF preservative-free lubricant eye drops nationwide due to lack of assurance of sterility following FDA observations during an inspection.

    Product
    OASIS TEARS PF — OASIS TEARS PF (GLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2148-2026·2026-05-20

    Medline Medical Convenience Kits with Namic Manifold Recalled

    Medline is recalling 107 medical convenience kits containing Namic Manifold (TAVI) due to particulate found in the fluid path. The kits were distributed nationwide and internationally.

    Product
    Medline medical convenience kits, containing Namic Manifold, Labeled as: TAVI, Medline Kit Number/SKU DYNJ904981C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2142-2026·2026-05-20

    Namic Preceptor Manifold extravascular blood pressure transducer

    Medline is recalling the Namic Preceptor Manifold due to particulate matter found in the fluid path. The recall affects 760 units distributed in the US and eight other countries.

    Product
    Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2167-2026·2026-05-20

    Hologic Selenia Dimensions Mammography Systems Loose Internal Bolts

    Hologic has recalled Selenia Dimensions Mammography Systems because internal bolts may become loose, missing, or broken over time. The company has received complaints of this issue affecting systems nationwide.

    Product
    SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2066-2026·2026-05-20

    Medical Angiographic Control Syringes Recalled for Rotating Adapter Risk

    Windstone Medical Packaging is recalling Custom Convenience Kits containing Medline Namic Angiographic Control Syringes due to risk that the rotating adapter may unwind during use, potentially causing disconnection and exposure to biohazards, blood loss, infection, or air embolism.

    Product
    Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2141-2026·2026-05-20

    Namic Preceptor Manifold blood pressure transducers recalled for particulate contamination

    Medline Industries is recalling Namic Preceptor Manifold extravascular blood pressure transducers due to the presence of particulate matter within the fluid path. The recall affects 6,390 units distributed nationwide in the US and internationally.

    Product
    Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2143-2026·2026-05-20

    Medline Medical Convenience Kits with Namic Manifold recalled

    Medline Industries is recalling medical convenience kits containing Namic Manifolds due to particulate matter found in the fluid path. The recall affects three kit models distributed nationwide and internationally.

    Product
    Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2144-2026·2026-05-20

    Medline Cardiac Catheterization Kits Recalled for Particulate Contamination

    Medline Industries is recalling multiple cardiac catheterization kits due to the presence of particulate matter in the fluid path of manifolds. The affected kits were distributed nationwide and internationally.

    Product
    1. DBD-MTS,3V,MAN,KIT, Medline Kit Number/SKU 60010195; 2. MTS-LEFT HEART,KIT, Medline Kit Number/SKU 60033123; 3. MTS,3 VALVE,KIT, Medline Kit Number/SKU 60050183; 4. MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60080349; 5. MTS,3 VALVE,LEFT HEART,KIT, Medline Kit Number/S
    Category
    Medical Device
    Distribution
    Distributed nationwide