Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 3,301–3,400, newest first.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1969-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1968-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1967-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1966-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1965-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1964-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1963-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1962-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1961-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1960-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1959-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1958-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1957-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1956-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1955-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1954-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1953-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1952-2026 · Official record ↗
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction …
Company / brand: Philips North America recalls
Official ID Z-1951-2026 · Official record ↗
The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin cell batter…
Company / brand: Advanced Bionics recalls
Official ID Z-1950-2026 · Official record ↗
It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settin…
Company / brand: Hologic recalls
Official ID Z-1949-2026 · Official record ↗
Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter Defibrillat…
Company / brand: Medtronic recalls
Official ID Z-1948-2026 · Official record ↗
Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the …
Company / brand: North American Rescue recalls
Official ID Z-1947-2026 · Official record ↗
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised…
Company / brand: Zimmer recalls
Official ID Z-1946-2026 · Official record ↗
Due to complaints of device breakage at the traction force gauge to handle joint.
Company / brand: Clinical Innovations recalls
Official ID Z-1945-2026 · Official record ↗
There is a possibility of reagent leakage from the specimen container.
Company / brand: Milestone S.R.L recalls
Official ID Z-1944-2026 · Official record ↗
Product does not have FDA clearance.
Company / brand: Healthmark Industries Co recalls
Official ID Z-1943-2026 · Official record ↗
Cyber vulnerability of BLE communication was found by CISA VDP program.
Company / brand: WHILL recalls
Official ID Z-1827-2026 · Official record ↗
Cyber vulnerability of BLE communication was found by CISA VDP program.
Company / brand: WHILL recalls
Official ID Z-1826-2026 · Official record ↗
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 an…
Company / brand: Boston Scientific recalls
Official ID Z-1771-2026 · Official record ↗
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 an…
Company / brand: Boston Scientific recalls
Official ID Z-1770-2026 · Official record ↗
product tested positive for Listeria Monocytogenes.
Company / brand: HEMU TRADING recalls
Official ID H-0686-2026 · Official record ↗
Product contains undeclared Yellow No. 5.
Company / brand: King Juice Company recalls
Official ID H-0685-2026 · Official record ↗
Foreign object found inside retail container.
Company / brand: The Mochi Ice Cream Company recalls
Official ID H-0684-2026 · Official record ↗
Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14.
Company / brand: Ganesha Enterprises recalls
Official ID H-0683-2026 · Official record ↗
Product may contain foreign objects, specifically glass.
Company / brand: LACTALIS CANADA recalls
Official ID H-0680-2026 · Official record ↗
Contains undeclared FD&C Yellow 6
Company / brand: Hadson (Toko) Trading Co recalls
Official ID H-0679-2026 · Official record ↗
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
Company / brand: Guangdong Zonegoing Food Co recalls
Official ID H-0678-2026 · Official record ↗
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
Company / brand: Guangdong Zonegoing Food Co recalls
Official ID H-0677-2026 · Official record ↗
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
Company / brand: Guangdong Zonegoing Food Co recalls
Official ID H-0676-2026 · Official record ↗
Undeclared allergen (almond).
Company / brand: Schreiber Foods recalls
Official ID H-0675-2026 · Official record ↗
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.
Company / brand: Hikma Pharmaceuticals USA recalls
Official ID D-0526-2026 · Official record ↗
Failed PH Specifications
Company / brand: Water-Jel Technologies recalls
Official ID D-0509-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0508-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0507-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0506-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0505-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0504-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0503-2026 · Official record ↗
cGMP deviations.
Company / brand: Wells Pharma of Houston recalls
Official ID D-0502-2026 · Official record ↗
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
Company / brand: Thea Pharma recalls
Official ID D-0501-2026 · Official record ↗
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
Company / brand: Thea Pharma recalls
Official ID D-0500-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: SCOPE HEALTH recalls
Official ID D-0499-2026 · Official record ↗
Labeling: Missing Label
Company / brand: American Regent recalls
Official ID D-0494-2026 · Official record ↗
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Company / brand: Alcon Research recalls
Official ID D-0492-2026 · Official record ↗
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Company / brand: Alcon Research recalls
Official ID D-0491-2026 · Official record ↗
Heat exposure may damage the hose. A damaged hose may leak fuel, increasing the risk of a fire.
Company / brand: Winnebago Industries recalls
Official ID 26V285000 · Official record ↗
Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
Company / brand: SHYFT Group recalls
Official ID 26V284000 · Official record ↗
A delayed rearview image reduces the driver's view behind the vehicle, increasing the risk of a crash.
Company / brand: Tesla recalls
Official ID 26V283000 · Official record ↗
An incorrect load carrying capacity label may lead to improper loading of the vehicle, increasing the risk of a crash.
Company / brand: Gulf States Toyota recalls
Official ID 26V282000 · Official record ↗
An instrument panel display that fails to show critical safety information, such as the speedometer and warning lights, increases the risk of a crash.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V281000 · Official record ↗
An incomplete seat may not properly restrain an occupant, increasing risk of injury during a crash.
Company / brand: Braun recalls
Official ID 26V280000 · Official record ↗
An unlit speedometer cannot show the vehicle's speed, increasing the risk of a crash.
Company / brand: New Flyer recalls
Official ID 26V279000 · Official record ↗
A passenger who is unable to fasten their seat belt is not properly restrained, increasing their risk of injury in a crash.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V278000 · Official record ↗
Entering a flooded roadway can cause a loss of vehicle control, increasing the risk of a crash or injury.
Company / brand: Waymo recalls
Official ID 26E026000 · Official record ↗
A loose base may allow the seat to move during a crash, increasing the risk of injury.
Company / brand: Grand Design RV recalls
Official ID 26V277000 · Official record ↗
A detached solar panel can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Grand Design RV recalls
Official ID 26V276000 · Official record ↗
An overloaded control unit may shutdown, causing a loss of drive power and increasing the risk of a crash.
Company / brand: Nova Bus recalls
Official ID 26V275000 · Official record ↗
The handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard.
Company / brand: American Honda Motor Co recalls
Official ID 26458 · Official notice ↗
The zipper slider on the side pouch can detach, posing a risk of serious injury or death from choking hazard to children.
Company / brand: Build-A-Bear Workshop recalls
Official ID 26457 · Official notice ↗
The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards.
Company / brand: CBC Group recalls
Official ID 26456 · Official notice ↗
The 6 mL nasal sprays contain an imidazoline, which must be in child-resistant packaging or meet the labeling requirements for non-complying packaging, as required by the Poison Pr…
Company / brand: Bayer HealthCare recalls
Official ID 26455 · Official notice ↗
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed…
Company / brand: Xiamen Fanlu Technology Co recalls
Official ID 26454 · Official notice ↗
A loose screw can cause the front tube to fold down unexpectedly, posing a risk of injury from a fall hazard.
Company / brand: Acer America recalls
Official ID 26453 · Official notice ↗
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
Company / brand: Ningbopingyao E-Commerce recalls
Official ID 26452 · Official notice ↗
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmer…
Company / brand: Shenzhen Qiangonghui Technology Co recalls
Official ID 26451 · Official notice ↗
The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death due to fall and injury …
Company / brand: Residential Elevators recalls
Official ID 26450 · 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…
Company / brand: Mobility Source Medical Technology Co recalls
Official ID 26449 · 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: UHOMEPRO recalls
Official ID 26448 · Official notice ↗
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed…
Company / brand: Shenzhen Maikeer Industrial Co recalls
Official ID 26447 · 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: SOFT recalls
Official ID 26446 · Official notice ↗
The pre-filled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Conta…
Company / brand: Alliance Chemical recalls
Official ID 26445 · Official notice ↗
If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in serious impact injury …
Company / brand: Thermos recalls
Official ID 26444 · Official notice ↗
A loss of drive power increases the risk of a crash.
Company / brand: Storyteller Overland recalls
Official ID 26V274000 · Official record ↗
Incorrect weight information can allow the vehicle to be overloaded, increasing the risk of a crash.
Company / brand: Newmar recalls
Official ID 26V273000 · Official record ↗
A detached spoiler may become a road hazard, increasing the risk of a crash.
Company / brand: Newmar recalls
Official ID 26V272000 · Official record ↗
A pop-top that lifts during transit can distract the driver, or detach if the secondary safety straps fail, increasing the risk of a crash.
Company / brand: Roadtrek recalls
Official ID 26V271000 · Official record ↗
The inability to shift into "Park" can result in a vehicle rollaway, increasing the risk of a crash.
Company / brand: Dorman Products recalls
Official ID 26E024000 · Official record ↗
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
Company / brand: Diversatek Healthcare recalls
Official ID Z-1941-2026 · Official record ↗
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
Company / brand: Diversatek Healthcare recalls
Official ID Z-1940-2026 · Official record ↗
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
Company / brand: Diversatek Healthcare recalls
Official ID Z-1939-2026 · Official record ↗
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
Company / brand: Diversatek Healthcare recalls
Official ID Z-1938-2026 · Official record ↗
Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys Hamilton STAR.
Company / brand: Foundation Medicine recalls
Official ID Z-1937-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1933-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1932-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1931-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1930-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1929-2026 · Official record ↗
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Company / brand: LSL Healthcare recalls
Official ID Z-1928-2026 · Official record ↗
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
Company / brand: Foundation Medicine recalls
Official ID Z-1927-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.