Wyoming recalls

Joly's 80% Vinegar sold on Amazon is missing required warning labels and safety instructions. The product can cause serious poisoning if swallowed or chemical burns if it contacts skin or eyes. About 450 bottles were sold between May and November 2025.

Huaker magnetic toy building sets sold on Amazon contain small balls that pose a serious choking hazard for children under 3 years old. These sets violate federal toy safety standards. About 782 sets were sold between September and November 2025.

Vive Health bed rails (models LVA1024 and LVA3031BLK) can trap users between the rail and mattress, creating a serious risk of entrapment and death by asphyxiation. The rails also lack required warning labels. About 12,355 units were sold online from August 2023 through December 2025.

Ajinomoto Foods North America is recalling frozen chicken fried rice products that may contain glass. The recall affects Ajinomoto Yakitori Chicken Fried Rice and Trader Joe's Chicken Fried Rice with specific best-by or best-before dates. The company discovered the problem after receiving four reports of glass found in the product, though no injuries have been confirmed.

Steris Corporation identified that a limited batch of MNA-6x0 adapter components used in the Barco MNA with HexaVue IP Integration System were manufactured with an incorrect configuration file. This affects 10 units with specific serial numbers distributed across seven states.

Surepulse Medical has recalled the VS Cap Extra Large component used in their VS Newborn Heart Rate Monitor because the labeling includes an incorrect sizing guide. This could lead to improper fit of the cap on the monitor. No injuries have been reported.

The labeling for the Surepulse VS Cap Large, a component of the VS Newborn Heart Rate Monitor, contains an incorrect sizing guide. This labeling error could lead to improper fit of the cap during use. No injuries have been reported.

Surepulse Medical has recalled the VS Cap Medium (part number SP-161-A1), a component of the VS Newborn Heart Rate Monitor, because the labeling contains an incorrect sizing guide. This labeling error could affect proper fit of the cap during use.

The labeling for the Surepulse VS Cap Small component of the VS Newborn Heart Rate Monitor contains an incorrect sizing guide. This affects specific lot numbers distributed in the US and several other countries. No injuries have been reported.

Surepulse Medical has recalled the VS Cap Extra Small (REF: SP-159-A1), a component of the VS Newborn Heart Rate Monitor, because the labeling includes an incorrect sizing guide. This labeling error could lead to improper cap selection for the device.

Certain da Vinci 5 Surgeon Console Viewer Displays have outdated firmware that may cause loss of the 3D surgical display or both displays entirely during surgery. When this happens, the surgical instruments remain active even though the surgeon cannot see the surgical field, which could result in unintended tissue contact, bleeding, or injury.

Philips Azurion 5 M20 X-ray imaging systems may move their patient table unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This could occur under certain conditions and pose a risk during medical procedures.

The table on certain Philips Azurion 5 M12 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This affects 326 units distributed worldwide, including 10 in the United States. No injuries have been reported.

Philips Azurion 7 M20 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This can occur under certain conditions across all software versions (R1.X, R2.X, R3.X). No injuries have been reported.

Philips medical imaging systems (Azurion 7 M12) may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This affects certain software versions across multiple model numbers. No injuries have been reported.

Philips medical imaging systems (Azurion 7 B20) may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is supposed to be engaged. This affects certain software versions across three model numbers distributed worldwide.

The examination table on certain Philips Azurion 7 B12 X-ray imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This could pose a safety risk to patients or staff during procedures. No injuries have been reported.

Philips medical imaging tables (Azurion 3 M15 systems) may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This affects specific model numbers with software versions R1.X, R2.X, and R3.X.

The table on certain Philips Azurion 3 M12 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This could create a safety risk in clinical settings. Philips has identified this issue and is working on a solution.

Alphatec Spine has recalled a surgical instrument (ATEC Lateral Navigation Disc Prep Osteotome 10mm) used in spine surgery procedures. The instrument has a design defect where the connection to the Medtronic navigation tracking system does not fit correctly, which could affect its safe operation during surgery.

Alphatec Spine has recalled its ATEC Lateral Navigation Disc Prep Osteotome (10mm, model 266-01-000-10-N) used in spinal surgery due to an incorrect connection geometry in the navigated array. This defect could affect how the instrument connects to the Medtronic StealthStation navigation system during surgery. Seven units were distributed across 14 U.S. states.

Certain Laerdal Compact Suction Unit 4 RTCA models made during a specific time period may emit electromagnetic noise above acceptable levels for aircraft use. No injuries have been reported. The affected units have specific catalog numbers: 880052, 880062, or 881152.

Elekta's Leksell GammaPlan treatment planning software (versions 11.3 and 11.4) has a software error that could cause incorrect treatment location data if users do not properly update reference settings. This could result in radiation therapy being directed to the wrong location if the error goes undetected.

Elekta's Leksell GammaPlan software version 11.1 has a bug that can cause incorrect radiation targeting during Gamma Knife treatment planning. If users don't update an old reference point before creating a new treatment plan, the radiation may be aimed at the wrong location. This error may not be caught during normal review.

Halyard TRANSPORT BAG KIT (Kit Code LIFE0080-01) may have a defective Tyvek bag seal that could compromise the sterility of the kit. The issue affects approximately 1,500 units distributed in New Jersey. No injuries have been reported.

Straumann USA LLC recalled certain WB Impression Post Closed Tray kits because they contain magenta impression caps instead of the correct brown caps. This mix-up could lead to using the wrong component during dental implant procedures. The recall affects 561 units distributed nationwide.

Medline Industries is recalling specific lots of Mercy Circumcision Tray kits because the BD ChloraPrep Triple Swabsticks inside may have open or compromised seals on their packaging. This could affect the sterility of the applicators before use. No injuries have been reported so far.

Medline is recalling specific lots of sterile resuture packs (SKU DYNDL1980A) because the BD ChloraPrep swabsticks inside may have broken seals on their packaging. An open seal could allow the swabs to become contaminated. No injuries have been reported.

Medline is recalling nine different medical convenience kits that contain BD ChloraPrep Triple Swabsticks with potentially compromised packaging seals. The affected applicators may have open or damaged seals, which could allow contamination. About 8,445 kits are involved nationwide.

Medline is recalling specific lots of its blood culture kits because the BD ChloraPrep Triple Swabsticks inside may have damaged or open packaging seals. This could allow the applicators to dry out or become contaminated before use. The affected lots are 25EBU508 and 25EBE330.