Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 2,701–2,800, newest first.
The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.
Company / brand: Tiny Land recalls
Official ID 26526 · Official notice ↗
The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support cushions because they can ob…
Company / brand: XJ Evermore recalls
Official ID 26525 · Official notice ↗
The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium ion battery's metal casing, causing the ba…
Company / brand: Wyze Labs recalls
Official ID 26524 · Official notice ↗
The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
Company / brand: Jayco recalls
Official ID 26V361000 · Official record ↗
The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
Company / brand: Jayco recalls
Official ID 26V360000 · Official record ↗
Brakes that overheat increase the risk of a fire.
Company / brand: Aston Martin The Americas recalls
Official ID 26V359000 · Official record ↗
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and b…
Company / brand: Medline Industries recalls
Official ID Z-2260-2026 · Official record ↗
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2259-2026 · Official record ↗
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2258-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2247-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2246-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2245-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2244-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2243-2026 · Official record ↗
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2242-2026 · Official record ↗
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2241-2026 · Official record ↗
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2240-2026 · Official record ↗
Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.
Company / brand: Devicor Medical Products recalls
Official ID Z-2239-2026 · Official record ↗
Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in cert…
Company / brand: Abiomed recalls
Official ID Z-2238-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2237-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2236-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2235-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2234-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2233-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2232-2026 · Official record ↗
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2231-2026 · Official record ↗
Nitrile Exam Glove failed to meet specifications chemical permeation performance.
Company / brand: O&M HALYARD recalls
Official ID Z-2230-2026 · Official record ↗
A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates have been implemented th…
Company / brand: Abiomed recalls
Official ID Z-2211-2026 · Official record ↗
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.
Company / brand: Bolton Medical recalls
Official ID Z-2160-2026 · Official record ↗
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0858-2026 · Official record ↗
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0857-2026 · Official record ↗
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0856-2026 · Official record ↗
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0855-2026 · Official record ↗
Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)
Company / brand: Fly By Jing recalls
Official ID H-0854-2026 · Official record ↗
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0852-2026 · Official record ↗
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0851-2026 · Official record ↗
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0850-2026 · Official record ↗
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
Company / brand: Honeyville recalls
Official ID H-0849-2026 · Official record ↗
Failed Stability Specifications
Company / brand: AbbVie recalls
Official ID D-0551-2026 · Official record ↗
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
Company / brand: AVEVA Drug Delivery Systems recalls
Official ID D-0550-2026 · Official record ↗
The unintended connection may prevent the air bags from deploying, increasing the risk of injury during a crash.
Company / brand: Braun recalls
Official ID 26V358000 · Official record ↗
Improperly restrained occupants have an increased risk of injury during a crash.
Company / brand: Braun recalls
Official ID 26V357000 · Official record ↗
A seat belt strap that does not extend can fail to restrain an occupant in a crash, increasing the risk of injury.
Company / brand: Kia America recalls
Official ID 26V356000 · Official record ↗
A low brake air pressure warning light that fails to illuminate when the engine is off will not alert the driver to a low brake pressure condition, increasing the risk of a crash i…
Company / brand: Nova Bus recalls
Official ID 26V355000 · Official record ↗
Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.
Company / brand: Grand Design RV recalls
Official ID 26V354000 · Official record ↗
A loose seat belt may not properly restrain an occupant during a crash, increasing the risk of injury.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V353000 · Official record ↗
The incorrect wiring may not make adequate contact, increasing the amperage and risk of a fire.
Company / brand: Forest River recalls
Official ID 26V352000 · Official record ↗
Wheel detachment can cause a loss of vehicle control or create a road hazard, increasing the risk of a crash or injury.
Company / brand: Mack Trucks recalls
Official ID 26V351000 · Official record ↗
Wheel detachment can cause a loss of vehicle control or create a road hazard, increasing the risk of a crash or injury.
Company / brand: Volvo Trucks North America recalls
Official ID 26V350000 · Official record ↗
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Arboc Specialty Vehicles recalls
Official ID 26V349000 · Official record ↗
A detach drive motor can become a road hazard for other vehicles, increasing the risk of a crash or injury.
Company / brand: International Motors recalls
Official ID 26V348000 · Official record ↗
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Forest River Bus recalls
Official ID 26V347000 · Official record ↗
A detached glass panel may become a road hazard, increasing the risk of a crash.
Company / brand: Subaru recalls
Official ID 26V346000 · Official record ↗
Inaccurate gear selection may result in unexpected vehicle movement, increasing the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V345000 · Official record ↗
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. Th…
Company / brand: Hop Thang Interior Wood Co recalls
Official ID 26522 · Official notice ↗
The recalled toys violate the mandatory safety standard for toys because the mini flashlight included with the fidget spinner balls contains button cell batteries that can be easil…
Company / brand: Shenzhenshibangduoladianzikejimaoyi Co recalls
Official ID 26515 · Official notice ↗
The racket sets violate the mandatory standard for toys because the screw on the racket used to secure the battery compartment does not remain attached when opened, and the button …
Company / brand: Missry Associates recalls
Official ID 26514 · Official notice ↗
The power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard.
Company / brand: Zhejiang Mingrui Furniture Co. aka Joy Furniture recalls
Official ID 26513 · Official notice ↗
Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk.
Company / brand: Giantex recalls
Official ID 26512 · Official notice ↗
The recalled sauna blankets can overheat, posing fire and burn hazards.
Company / brand: Tzumi Electronics of New York recalls
Official ID 26511 · Official notice ↗
The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin batteries are swallowed, th…
Company / brand: Proudly American Store recalls
Official ID 26510 · Official notice ↗
The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets a…
Company / brand: Daoen recalls
Official ID 26509 · Official notice ↗
The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than permitted, posing a dead…
Company / brand: MiniWarGaming recalls
Official ID 26508 · Official notice ↗
The sauna's steam diffuser can be positioned too close to a consumer's body, allowing hot steam to come in contact with user, posing a burn hazard.
Company / brand: Giantex recalls
Official ID 26506 · Official notice ↗
Seat belts that do not retract or extend can fail to restrain an occupant as intended, increasing the risk of injury in a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V344000 · Official record ↗
A sudden loss of drive power can increase the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V343000 · Official record ↗
The incorrect label color may make it difficult for the operator to locate the loading or tire pressure information, increasing the risk of a crash.
Company / brand: Tiffin Motorhomes recalls
Official ID 26V342000 · Official record ↗
An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V341000 · Official record ↗
A detached control arm can cause a loss of vehicle control, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V340000 · Official record ↗
Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.
Company / brand: Ember Recreational Vehicles recalls
Official ID 26V339000 · Official record ↗
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2229-2026 · Official record ↗
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2228-2026 · Official record ↗
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2227-2026 · Official record ↗
Due to stain present on the surface of affected foley catheters.
Company / brand: C.R. Bard recalls
Official ID Z-2226-2026 · Official record ↗
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the c…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2225-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2222-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2221-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2220-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2219-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2218-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2217-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2216-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2215-2026 · Official record ↗
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2214-2026 · Official record ↗
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, …
Company / brand: Novapproach Spine recalls
Official ID Z-2213-2026 · Official record ↗
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy …
Company / brand: ICU Medical recalls
Official ID Z-2210-2026 · Official record ↗
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Company / brand: TANGENT ENDOSCOPY recalls
Official ID Z-2209-2026 · Official record ↗
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2204-2026 · Official record ↗
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2203-2026 · Official record ↗
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2202-2026 · Official record ↗
Product may be contaminated with Salmonella.
Company / brand: Stoltzfus Family Dairy recalls
Official ID H-0848-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0847-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0846-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0845-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0844-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0843-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0842-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0841-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0840-2026 · Official record ↗
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0839-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.