Florida recalls

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.

Publix is recalling all lots of GreenWise Organic Whole Blueberries and Whole Mixed Berries (10-oz and 48-oz packages) due to potential contamination with E. coli O145, a strain that can cause severe stomach cramps, diarrhea, and vomiting. The affected products were sold in Publix stores across eight states: Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia.

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.

The Olympus UHI-4 insufflation unit may experience unexpected shutdowns where the front panel display turns off and air delivery stops during use. This affects about 3,087 units distributed worldwide. No injuries have been reported.

The SnapshotGLO device's software cannot recognize when its battery has fully discharged into a low-power shipping mode. When this happens, the device will not resume charging when plugged in and becomes temporarily unusable until the issue is corrected.

Micro Therapeutics Pipeline Flex Embolization Devices have incorrect labeling on some units. Devices labeled as 3.0 mm x 20 mm actually contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm actually contain 20 mm implants. This mismatch could lead to incorrect implant selection during surgery.

Certain Halyard STANDARD LINE INSERTION PACK kits (Model PVHM234-01) have a defect in the silicone seal that may not seal properly. This defect can cause the seal to dome inward, potentially blocking fluid flow or allowing fluid to leak where it shouldn't.

The TheraSphere 360 Y-90 Management Platform has a software bug that can cause incorrect dose calculations. When a user modifies calculation inputs and recalculates, the new dose is computed correctly on screen, but vials previously added to the cart do not automatically update to match the revised calculation.