Oregon recalls

Curry Chicken Salad products produced on July 22, 2026 may be contaminated with Listeria monocytogenes. The affected 8-oz packages have a use-by date of 07/30/2026 and were shipped to retail locations in Oregon and Washington. No illnesses have been reported.

Woodure tower step stools can collapse or tip over during use. Children's torsos can fit through openings on the front and back, creating a risk of entrapment, falls, and serious injury. The company has received 22 reports of tip-overs, including 15 injuries.

This baby doll playset includes small accessories like a pacifier, spoon, toothbrush, and soap dish that can be swallowed by young children. The toy is marketed for children under three years old but contains parts small enough to choke on, violating federal safety rules.

Mangohood Direct kids kitchen tower stools (model LT003) can collapse or tip over during use. The openings on the front and back are large enough for a child's torso to fit through, creating a serious risk of entrapment, falls, and injury.

Jake's Fireworks World Class Fireworks "Skull Strobe" rockets can explode before reaching their intended height, creating serious explosion and burn hazards. The wooden-stick rockets were sold at fireworks retailers nationwide between March 2025 and June 2026. No injuries have been reported.

The electrical cord on OCTROT heated throws and blankets can detach and ignite, creating a fire hazard. The company has received reports of 27 fires and 15 burn or electrical shock injuries linked to the product.

HARPPA's Nordi toddler tower stools can collapse or tip over during use. The stools have openings on the front and back that are large enough for a child's torso to fit through, creating a risk of entrapment. The company has received three reports of stools collapsing or tipping, resulting in injuries including scrapes, cuts, and bruises.

Golden Link sold Fantastic Four drinking cups and Captain America popcorn helmet containers with LED lights at movie theaters. The products contain easily accessible button cell batteries that children can swallow, which can cause serious internal burns or death. The products also lack required warning labels.

Galanz retro-style refrigerators sold from 2019 to 2022 can develop electrical short circuits that ignite, creating a fire and burn risk. The company has received 34 reports of fires, including one that resulted in a death.

The rechargeable lithium-ion battery in BenQ GV31 portable projectors can overheat, creating a risk of fire and burns. BenQ has received three reports of overheating, including one case of hand burns. About 1,249 projectors are affected in the U.S.

KAIFAM 5-drawer dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards for furniture stability. About 1,980 units were sold online.

EnHomee 15-Drawer Dressers sold on Amazon can tip over and trap children if they are not anchored to the wall. The dressers do not meet federal safety standards for clothing storage units. About 12,800 units were sold between August 2024 and April 2026.

Trsmima backyard zipline kits sold on Amazon can fail during use in dangerous ways: the steel cable, seat, or turnbuckle can detach or break, causing falls; and the spring brakes don't slow riders safely, leading to collisions with trees or falls. At least 21 people have been injured, including fractures and concussions.

Karl Storz Flexible Hystero-Fiberscope Kits with certain serial numbers contain expired single-use endoscopic seals that may not maintain sterility during gynecological procedures. The affected seals expired in January 2023 and were distributed across 15 U.S. states.

The SafeOp Patient Interface (REF: AIX11240), part of the SafeOp 3 Neural Informatix System used during spine surgery, can lose or drop its nerve monitoring signal due to a software problem. When this happens, the device may show system errors, lose connection to the surgeon's tablet, and require a restart—potentially extending surgery time or changing the surgical plan.

Medline Industries is recalling nine types of surgical convenience kits that contain BD PurPrep solution. The solution may be contaminated with low levels of Bacillus species, a bacterium that could pose a risk if the kits are used in sterile procedures. The recall affects specific lot numbers of joint, spine, and neurological surgery kits distributed to hospitals and surgical centers in ten U.S. states.

Medline Industries recalled specific NEURO PACK medical convenience kits because the included BD PurPrep 26 mL solution may contain low levels of Bacillus species bacteria. The contamination was identified in kits distributed to hospitals and medical facilities in 10 U.S. states.

Medline Industries is recalling three types of medical convenience kits (Shoulder Pack and Major Ortho Kit models) because the BD PurPrep solution included in them may contain low levels of Bacillus species bacteria. The contamination was discovered in specific lot numbers distributed across ten U.S. states.

Medline Industries is recalling specific pediatric open heart and cardiac surgical convenience kits that contain BD PurPrep solution potentially contaminated with low levels of Bacillus species. The affected kits were distributed to healthcare facilities in 10 states. No injuries have been reported.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could potentially be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled. The catheters contain increased amounts of raw material on the surface, which may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) include catheters with excess raw material on the surface. This material may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled due to increased raw material on the catheter surface. This contamination may cause staining and could potentially be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful to patients.

Medline convenience kits used in urology robotic procedures contain Bard Silastic Foley Catheters with excess raw material on the catheter surface. This material may cause staining and could potentially harm patients. The catheters were originally recalled by the manufacturer due to this manufacturing defect.

Medline convenience kits containing Bard Silastic Foley Catheters have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful if the catheters are used.

Medtronic MiniMed Go app versions 1.0.0 and 1.1.0 have a software bug: when the "Set day and night" feature is turned off, missed-dose and high-glucose alerts may fail to trigger at night. This means users may not realize they've missed insulin doses, potentially delaying treatment and raising blood sugar levels dangerously.

Emano Flow, a smartphone app that measures urinary flow rate and volume, produced inaccurate results during a two-month period (March 22–May 29, 2026). The app recorded audio at an incorrect frequency setting, causing measurements to be systematically over-reported. The company has provided corrected results to healthcare teams.