Search 318 recent U.S. safety recalls from the CPSC, NHTSA, and FDA — updated hourly, with the official government notice one click from every result.
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…
Official ID 26630 · Official notice ↗
The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.
Official ID 26629 · Official notice ↗
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and d…
Official ID 26628 · Official notice ↗
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…
Official ID 26627 · Official notice ↗
The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or dea…
Official ID 26626 · Official notice ↗
The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.
Official ID 26625 · Official notice ↗
The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.
Official ID 26624 · Official notice ↗
The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cau…
Official ID 26623 · Official notice ↗
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…
Official ID 26622 · Official notice ↗
The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard.
Official ID 26621 · Official notice ↗
The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards.
Official ID 26620 · Official notice ↗
The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the?Poison Prevention Packaging Act. The bottles are not …
Official ID 26619 · Official notice ↗
The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.
Official ID 26618 · Official notice ↗
The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin…
Official ID 26617 · Official notice ↗
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.
Official ID Z-2717-2026 · Official notice ↗
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
Official ID Z-2716-2026 · Official notice ↗
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
Official ID Z-2715-2026 · Official notice ↗
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 …
Official ID Z-2714-2026 · Official notice ↗
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.
Official ID Z-2713-2026 · Official notice ↗
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Official ID Z-2712-2026 · Official notice ↗
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Official ID Z-2711-2026 · Official notice ↗
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Official ID Z-2710-2026 · Official notice ↗
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patien…
Official ID Z-2703-2026 · Official notice ↗
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.
Official ID Z-2702-2026 · Official notice ↗
CPSC recallsNHTSA recallsFDA recalls
Consumer Product (133)Medical device (60)Drug (60)Food (60)Vehicle (5)
Data last assembled July 23, 2026 at 8:06 PM UTC. Fresh Recalls mirrors official public-domain government data and always links the original notice.