Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 401–500, newest first.
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Company / brand: Midmark recalls
Official ID Z-3217-2026 · Official record ↗
Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,
Company / brand: Olympus of the Americas recalls
Official ID Z-3216-2026 · Official record ↗
Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand. The stand may tip over as a result. Falling stand m…
Company / brand: Heidelberg Engineering recalls
Official ID Z-3215-2026 · Official record ↗
Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature. Patient impact may include prolonged procedure or life-th…
Company / brand: Boston Scientific recalls
Official ID Z-3214-2026 · Official record ↗
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.
Company / brand: AVID Medical recalls
Official ID Z-3194-2026 · Official record ↗
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu…
Company / brand: CooperSurgical recalls
Official ID Z-3140-2026 · Official record ↗
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu…
Company / brand: CooperSurgical recalls
Official ID Z-3139-2026 · Official record ↗
Contamination with Listeria monocytogenes
Company / brand: GIAS FOOD recalls
Official ID H-1396-2026 · Official record ↗
Undeclared Egg Allergen
Company / brand: WFM Purchasing recalls
Official ID H-1395-2026 · Official record ↗
Product may contain foreign material: small stones and other hard objects.
Company / brand: WWF Operating Company recalls
Official ID H-1394-2026 · Official record ↗
Potential contamination with pesticides.
Company / brand: Kwok Shing recalls
Official ID H-1393-2026 · Official record ↗
Potential Wheat Kernel contamination.
Company / brand: United Sugar Producers and Refiners recalls
Official ID H-1392-2026 · Official record ↗
Potential Wheat Kernel contamination.
Company / brand: United Sugar Producers and Refiners recalls
Official ID H-1391-2026 · Official record ↗
Salmonella
Company / brand: Evergreen Fresh Sprouts recalls
Official ID H-1390-2026 · Official record ↗
Potential Listeria contamination from dripping condensation in cooler.
Company / brand: Elegant Foods recalls
Official ID H-1389-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Insight Pharmaceuticals recalls
Official ID D-0871-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Insight Pharmaceuticals recalls
Official ID D-0870-2026 · Official record ↗
Defective Delivery System: Possibility of no medication in the prefilled pen.
Company / brand: Amneal Pharmaceuticals of New York recalls
Official ID D-0868-2026 · Official record ↗
Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.
Company / brand: Macleods Pharmaceuticals recalls
Official ID D-0867-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0863-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0862-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0861-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0860-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0859-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0858-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0857-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0856-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Sterling Pharmaceutical Services recalls
Official ID D-0855-2026 · Official record ↗
cGMP Deviations
Company / brand: SHANTOU Qiwei industrial Co recalls
Official ID D-0854-2026 · Official record ↗
A loss of drive power increases the risk of a crash.
Company / brand: Rivian Automotive recalls
Official ID 26V625000 · Official record ↗
A detached bike rack can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Nova Bus recalls
Official ID 26V624000 · Official record ↗
A TPMS warning light that fails to notify the driver of low tire pressure increases the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V623000 · Official record ↗
A side air bag that does not deploy as intended increases the risk of injury in a crash.
Company / brand: Chrysler recalls
Official ID 26V622000 · Official record ↗
A loss of power steering assist can increase the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V621000 · Official record ↗
A loss of power steering assist can increase the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26E067000 · Official record ↗
Reduced braking performance can require a greater distance to stop, increasing the risk of a crash.
Company / brand: Mack Trucks recalls
Official ID 26V620000 · Official record ↗
Reduced braking performance can require a greater distance to stop, increasing the risk of a crash.
Company / brand: Volvo Trucks North America recalls
Official ID 26V619000 · Official record ↗
A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
Company / brand: Cummins recalls
Official ID 26E066000 · Official record ↗
A separated trailer coupler can cause a loss of control and increase the risk of a crash.
Company / brand: Aluminum Trailer Company recalls
Official ID 26V618000 · Official record ↗
When the vehicle is moved or driven with the boom out of stow, the vehicle could exceed the recorded travel height, increasing the risk of a crash.
Company / brand: Altec Industries recalls
Official ID 26V617000 · Official record ↗
While damage to the power center increases the risk of a fire, damage to the electrical system may cause the trailer brakes or exterior lightings to fail, increasing the risk of a …
Company / brand: Grand Design RV recalls
Official ID 26V616000 · Official record ↗
An improperly stitched seat belt may fail to properly restrain an occupant during a crash, increasing the risk of injury.
Company / brand: Jaguar Land Rover North America recalls
Official ID 26V615000 · Official record ↗
A cracked subframe may have reduced structural integrity, increasing the risk of injury during a crash. A crack may also diminish handling and control, increasing the risk of a cra…
Company / brand: Jaguar Land Rover North America recalls
Official ID 26V613000 · Official record ↗
A closing window that does not reverse direction as expected can pinch a passenger before retracting, increasing the risk of injury.
Company / brand: General Motors recalls
Official ID 26V612000 · Official record ↗
A detached end cap or inflator rupture can allow compressed gas to escape and project the end cap or fragments of the inflator into the vehicle, increasing the risk of injury.
Company / brand: General Motors recalls
Official ID 26V611000 · Official record ↗
The recalled children’s toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed …
Company / brand: ABC Trading recalls
Official ID 26799 · Official notice ↗
The lithium-ion battery in the recalled portable sleep machines can overheat if the charger is not compatible with the unit, posing a risk of injury from fire and burn hazards.
Company / brand: Love To Dream recalls
Official ID 26798 · Official notice ↗
The left temple of the recalled smart glasses can overheat during extended use, posing a risk of serious injury or death due to burn hazard.
Company / brand: INMO International Technology recalls
Official ID 26797 · Official notice ↗
The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
Company / brand: Sold Online At: Amazon.com from January 2026 through May 2026 for $226. Style Homeware recalls
Official ID 26796 · 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…
Company / brand: Dongguan Meiying Sen Smart Home Co recalls
Official ID 26794 · Official notice ↗
The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
Company / brand: Huizhou Xiqijun Trading Co recalls
Official ID 26793 · Official notice ↗
The lithium-ion battery in the power banks can explode or ignite, posing fire and burn hazards to consumers.
Company / brand: Shenzhen Xinkewangda Electronics Co recalls
Official ID 26792 · Official notice ↗
The lithium-ion battery in the recalled battery packs can overheat, posing fire and burn hazards to consumers.
Company / brand: Go North Rocket 28 AB recalls
Official ID 26791 · Official notice ↗
The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Contain…
Company / brand: Sold At: The Asylum Automotive Store in Houston recalls
Official ID 26790 · Official notice ↗
The helmets in the recalled sets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, retention system, position…
Company / brand: Sold Online At: Amazon.com in May 2026 for between $25 and $26. Hengqin Guangwei Consulting Co recalls
Official ID 26789 · Official notice ↗
The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
Company / brand: S-Q Business (HK) recalls
Official ID 26788 · Official notice ↗
A misaligned mat may not be supported, resulting in an occupant falling from the bunk and increasing the risk of injury.
Company / brand: Forest River recalls
Official ID 26V610000 · Official record ↗
A ladder that pulls away from the bunk increases the risk of injury.
Company / brand: Forest River recalls
Official ID 26V609000 · Official record ↗
A blocked door can prevent or delay occupants from exiting during an emergency, increasing their risk of injury.
Company / brand: Forest River recalls
Official ID 26V608000 · Official record ↗
A deformed circuit board may cause a loss of drive power, increases the risk of a crash.
Company / brand: Jaguar Land Rover North America recalls
Official ID 26V607000 · Official record ↗
Failed Stability Specifications
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID EVT-99876-z42zg7 · Official record ↗
undeclared ingredients including but not limited to mustard
Company / brand: KRAFT HEINZ FOODS COMPANY recalls
Official ID EVT-99869-14pecqd · Official record ↗
Transfemoral catheter, positing arm may detached due to weld issue.
Company / brand: PI CARDIA recalls
Official ID Z-3213-2026 · Official record ↗
Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, expo…
Company / brand: ICU Medical recalls
Official ID Z-3212-2026 · Official record ↗
Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.
Company / brand: F & A Foundation recalls
Official ID Z-3211-2026 · Official record ↗
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…
Company / brand: Medline Industries recalls
Official ID Z-3210-2026 · Official record ↗
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…
Company / brand: Medline Industries recalls
Official ID Z-3209-2026 · Official record ↗
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…
Company / brand: Medline Industries recalls
Official ID Z-3208-2026 · Official record ↗
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…
Company / brand: Medline Industries recalls
Official ID Z-3207-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3206-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3205-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3204-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3203-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3202-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3201-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3200-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3199-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3198-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3197-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3196-2026 · Official record ↗
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…
Company / brand: Howmedica Osteonics recalls
Official ID Z-3195-2026 · Official record ↗
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.
Company / brand: Mirion Technologies (Capintec) recalls
Official ID Z-3193-2026 · Official record ↗
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…
Company / brand: Datex-Ohmeda recalls
Official ID Z-3192-2026 · Official record ↗
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…
Company / brand: Datex-Ohmeda recalls
Official ID Z-3191-2026 · Official record ↗
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…
Company / brand: Datex-Ohmeda recalls
Official ID Z-3190-2026 · Official record ↗
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…
Company / brand: Datex-Ohmeda recalls
Official ID Z-3189-2026 · Official record ↗
A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail elect…
Company / brand: Boston Scientific recalls
Official ID Z-3188-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3187-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3186-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3185-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3184-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3183-2026 · Official record ↗
Reusable access port system may crack or seperate during use.
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-3182-2026 · Official record ↗
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the componen…
Company / brand: Medical Action Industries recalls
Official ID Z-3181-2026 · Official record ↗
Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.
Company / brand: embecta Medical II recalls
Official ID Z-3180-2026 · Official record ↗
Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.
Company / brand: embecta Medical II recalls
Official ID Z-3179-2026 · Official record ↗
Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fix…
Company / brand: restor3d recalls
Official ID Z-3178-2026 · Official record ↗
Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU).
Company / brand: Wilson-Cook Medical recalls
Official ID Z-3177-2026 · Official record ↗
Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.
Company / brand: Happiest Baby recalls
Official ID Z-3176-2026 · Official record ↗
Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.
Company / brand: Happiest Baby recalls
Official ID Z-3175-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.