Alaska recalls

Sold nationwide. BD is recalling specific lots of its Intraosseous Vascular Access System Needle Sets because some users have had difficulty removing the obturator (stylet) after needle placement. The affected needle sets were manufactured with out-of-tolerance dimensions and distributed between September 2024 and June 2026. If the obturator cannot be removed, clinicians may need to obtain alternative vascular access, potentially delaying urgent care.

Serious·FDA·Jul 30, 2026·BD

Sold nationwide. The lithium-ion batteries in OCOOPA-branded rechargeable hand warmers can overheat and catch fire, causing serious burns. About 1.5 million units sold online are affected, including models UT3053, UT3056, ZLS-118, ZLS-118S, ZLS-118D, H01, and H01(PD). One death and multiple burn injuries have been reported.

Serious·CPSC·Jul 30, 2026·OCOOPA

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Segmart

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·TOYHW

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Mangohood Direct

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Jake's Fireworks

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·OCTROT

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Harppa

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Golden Link

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Galanz

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·BenQ

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·KAIFAM

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Jiaxuan

Sold nationwide. 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.

Serious·CPSC·Jul 30, 2026·Trsmima

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Karl Storz

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Alphatec Spine

Sold nationwide. Medline is recalling nine urology convenience kits that contain Bard Silastic Foley catheters. The catheter maker recalled them because they have higher than intended amounts of raw material on the surface, which can cause staining and may be harmful. The kits were distributed nationwide, with confirmed distribution in California, Florida, Maryland, Pennsylvania, and Texas, and no injuries have been reported.

Moderate·FDA·Jul 29, 2026·Medline9 products

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Medtronic

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Emano Metrics

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Olympus

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Kent Imaging

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Micro Therapeutics2 products

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·AVID Medical

Sold nationwide. 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.

Moderate·FDA·Jul 29, 2026·Boston Scientific

Sold nationwide. Penumbra System RED 68 Reperfusion Catheters (REF: RED68KIT) may fracture during use due to a manufacturing defect. The affected lots are H00008699, H00008701, H00008702, H00008703, and C00020038. These catheters were distributed worldwide, including throughout the United States.

Serious·FDA·Jul 29, 2026·Penumbra

Sold nationwide. Prismatik Dentalcraft distributed Silent Nite Sleep Appliances (a mandibular advancement device for snoring and sleep apnea) without obtaining required FDA clearance. The devices were sold in multiple states before the clearance status was identified.

Moderate·FDA·Jul 29, 2026·Prismatik Dentalcraft

Sold nationwide. Medtronic Neurosurgery's Ventriculostomy Kit (REF: 46154) may contain endotoxin levels higher than safe limits for devices that contact cerebrospinal fluid during brain surgery. Endotoxin exposure can trigger acute inflammation in the brain and nervous system.

Moderate·FDA·Jul 29, 2026·Medtronic

Sold nationwide. The 3mensio Workstation software may report heart and vessel measurements that are 0.8% to 34% larger than the actual size when specific conditions are met: the software is used with access only to 3D Echo or Mitral 3D Echo features, and the analysis involves Philips 3D echo datasets that contain Color Doppler data. This could lead to incorrect clinical measurements used in patient care decisions.

Moderate·FDA·Jul 29, 2026·PIE Medical Imaging

Sold nationwide. Certain Halyard EYE PACK convenience kits (Model LVEY27) contain Betadine solution at an incorrect concentration. The kits were distributed nationwide, primarily in California. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·AVID Medical

Sold nationwide. SeaSpine Orthopedics has recalled certain Polyaxial Head spinal implants (REF 41-3010) due to a manufacturing error that may cause the polyaxial head to detach from the screw during surgery after insertion. This could require additional surgical intervention. The recall affects 796 units distributed worldwide, including nationwide US distribution and locations in Chile and Australia.

Moderate·FDA·Jul 29, 2026·SeaSpine