State
73,096 recalls have nationwide distribution and so reach Wyoming. 3,226 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,226 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 549 (17%) are Severe.
Which agencies issued them
These figures cover only the 3,226 recalls whose distribution notice names Wyoming specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Firefly Integrations is recalling specific G12 Electronic Control Modules installed in Thor Motor Coach vehicles due to a software error that may allow the awning to extend while driving.
Thy Trading Company recalls approximately 720 roll-up window blinds sold on Wayfair.com due to long operating cords that pose strangulation and entanglement hazards to children. Consumers should stop using the blinds immediately and request a full refund.
UVIPC Baby Gates sold on Amazon have been recalled due to an entrapment hazard that violates federal safety regulations, as children's torsos can fit through gaps in the gate design. No injuries have been reported.
TravisMathew recalled approximately 59,450 women's and men's hoodies and sweatshirts sold from January through October 2024 due to violation of federal flammability standards, posing a burn hazard.
Pella Corporation is recalling about 340 Pella Reserve and Lifestyle sliding patio doors and windows because their sensor panels and remote controls contain button cell batteries that children can easily access, posing an ingestion hazard.
Ariens snow throwers may continue rotating after the operator releases the control lever, creating a laceration hazard. The company is offering free repairs at authorized dealers.
Doosan Bobcat is recalling about 552 AirFX Finish Mower Deck attachments because the locking pins may fail to secure the deck during maintenance, creating a crush hazard. No injuries have been reported.
Astellas Pharma recalls Prograf (tacrolimus) 0.5 mg capsules distributed nationwide due to empty capsules in bottles. Affected lot 0E3353D expires March 31, 2026.
Samsung SDI is recalling high-voltage battery packs installed in Chrysler, Volkswagen/Audi, and Ford vehicles because they may fail, increasing the risk of a crash or fire.
Medline arterial line tray kits (models ART600 and ART690) are being recalled because the catheter hub contains excess material from manufacturing. The recall affects 58 kits distributed nationwide.
Medline Industries is recalling 942 arterial line insertion kits due to excess material on the catheter hub of the catheter subassembly. The manufacturing defect prompted a FDA Class I recall of products distributed nationwide.
The Mochi Ice Cream Company is recalling My Mochi Sorbet Peach Mango Sorbet nationwide due to undeclared egg allergen. Consumers with egg allergies should not consume this product.
Astellas Pharma is recalling Astagraf XL (tacrolimus) due to manufacturing defects; bottles shipped nationwide may contain empty capsules instead of medication.
Zimmer, Inc. is recalling 155 units of NexGen LCCK Legacy knee implant components because the metal support post was assembled incorrectly in some units. The defective assembly could compromise implant function.
Medtronic is recalling sterile percutaneous reference pins used in image-guided surgery because the pins may not fit into the patient reference frame or adapter, potentially affecting proper surgical tracking.
Karl Storz is recalling its Ureteroscope (Model 27001K) because the Instructions for Use contain reprocessing procedures that have not been reviewed or approved by the FDA. All 185 units distributed nationwide are affected.
Karl Storz is recalling 185 Pediatric Cysto-Urethroscope instruments nationwide. The product instructions contain reprocessing methods that have not been reviewed or approved by the FDA for safety and effectiveness.
The AXIOS Stent and Delivery System is being recalled because the outer sheath can detach and prevent proper stent expansion, requiring device replacement during the procedure.
The HOT AXIOS Stent delivery system's outer sheath tip may detach during use, preventing proper stent expansion and requiring device exchange. Boston Scientific is recalling 1,102 units distributed nationwide.
Honda is recalling certain 2025 Pilot vehicles because the third-row passenger seat belt may not function due to incorrect routing. A non-functioning seat belt cannot properly restrain occupants, increasing injury risk during a crash.
Karl Storz ureteroscopes contain reprocessing instructions that have not been reviewed and approved by the FDA. Affected devices should not be reprocessed using unapproved methods.
Boston Scientific's HOT AXIOS stent delivery system has a defect where the outer sheath can detach and prevent proper stent expansion, requiring device replacement.
The muRata Vios Monitoring System Model 2050 bedside cardiac monitor has been recalled due to a software issue causing patient vital signs and ECG waveforms to flicker and become distorted on the Central Station Monitor. No injuries have been reported.
Boston Scientific is recalling HOT AXIOS Stent systems because the outer sheath's tip can detach and prevent proper stent expansion, requiring device replacement during procedures.
Karl Storz is recalling a uretero-renoscope surgical device (REF 27003L) because the reprocessing instructions in the product documentation have not been reviewed or approved by the FDA.