Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,901–2,000, newest first.
The electrical system may overheat without a ground, increasing the risk of a fire. There is also an increased risk of injury from electrical shock.
Company / brand: Jayco recalls
Official ID 26V426000 · Official record ↗
An improperly secured child restraint system may not restrain an occupant as intended, increasing the risk of injury during a crash.
Company / brand: Nissan North America recalls
Official ID 26V425000 · Official record ↗
A winch that operates unintentionally may increase the risk of injury.
Company / brand: Warn Industries recalls
Official ID 26E041000 · Official record ↗
The recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards.
Company / brand: Winco Fireworks International recalls
Official ID 26603 · Official notice ↗
The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards.
Company / brand: Winco Fireworks International recalls
Official ID 26602 · Official notice ↗
Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
Company / brand: Conair recalls
Official ID 26601 · Official notice ↗
The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin batteries are swallo…
Company / brand: Changzhou Niujie Battery Technology Co recalls
Official ID 26600 · Official notice ↗
The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.
Company / brand: Cooper Lighting recalls
Official ID 26599 · Official notice ↗
The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard.
Company / brand: Target recalls
Official ID 26598 · 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: Xishentang Dongguan Trading Co recalls
Official ID 26596 · Official notice ↗
The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
Company / brand: Groupe SEB USA dba Rowenta USA recalls
Official ID 26595 · Official notice ↗
The recalled LED 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 …
Company / brand: Shenzhen Bopu Product Design Co recalls
Official ID 26594 · Official notice ↗
The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not ch…
Company / brand: Diamond Wipes International recalls
Official ID 26593 · Official notice ↗
The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning …
Company / brand: Changsha Jiali Duo Technology Co recalls
Official ID 26592 · Official notice ↗
The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed openings at the foot of the …
Company / brand: Sanven Technology recalls
Official ID 26591 · Official notice ↗
Loose rear subframe bolts can lead to a loss of vehicle stability or rear subframe detachment, increasing the risk of a crash or injury.
Company / brand: Honda recalls
Official ID 26V424000 · Official record ↗
A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
Company / brand: Honda recalls
Official ID 26V423000 · Official record ↗
A loss of power brake assist can extend the distance required to stop the vehicle. Additionally, malfunctioning ABS and/or DSC systems can cause a loss of vehicle control. Either…
Company / brand: BMW Of North America recalls
Official ID 26V422000 · Official record ↗
Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V421000 · Official record ↗
Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26E040000 · Official record ↗
Potential for thrombus formation during prolonged use of the introducer.
Company / brand: Abiomed recalls
Official ID Z-2602-2026 · Official record ↗
Potential for thrombus formation during prolonged use of the introducer.
Company / brand: Abiomed recalls
Official ID Z-2601-2026 · Official record ↗
Potential for thrombus formation during prolonged use of the introducer.
Company / brand: Abiomed recalls
Official ID Z-2600-2026 · Official record ↗
Potential for thrombus formation during prolonged use of the introducer.
Company / brand: Abiomed recalls
Official ID Z-2599-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2596-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2595-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2594-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2593-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2592-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2591-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2590-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2589-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2588-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2587-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2586-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2585-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2584-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2583-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2582-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries recalls
Official ID Z-2581-2026 · Official record ↗
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Company / brand: Boston Scientific recalls
Official ID Z-2580-2026 · Official record ↗
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PI…
Company / brand: Philips North America recalls
Official ID Z-2579-2026 · Official record ↗
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Company / brand: Zimmer recalls
Official ID Z-2578-2026 · Official record ↗
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2577-2026 · Official record ↗
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2576-2026 · Official record ↗
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2575-2026 · Official record ↗
Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies …
Company / brand: Dexcom recalls
Official ID Z-2574-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2573-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2572-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2571-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2570-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2569-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2568-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2567-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2566-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2565-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2564-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2563-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2562-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2561-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2560-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2559-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2558-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2557-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2556-2026 · Official record ↗
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Official ID Z-2555-2026 · Official record ↗
Software anomaly that causes a false display of error code 5018.
Company / brand: IPG Medical recalls
Official ID Z-2554-2026 · Official record ↗
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches…
Company / brand: GE Medical Systems SCS recalls
Official ID Z-2553-2026 · Official record ↗
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be …
Company / brand: Stryker Neurovascular recalls
Official ID Z-2552-2026 · Official record ↗
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
Company / brand: Acumed recalls
Official ID Z-2532-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Company / brand: Zimmer recalls
Official ID Z-2531-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Company / brand: Zimmer recalls
Official ID Z-2530-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Company / brand: Zimmer recalls
Official ID Z-2529-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Company / brand: Zimmer recalls
Official ID Z-2528-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Company / brand: Zimmer recalls
Official ID Z-2527-2026 · Official record ↗
A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-…
Company / brand: PFM MEDICAL recalls
Official ID Z-2526-2026 · Official record ↗
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the back…
Company / brand: Ventec Life Systems recalls
Official ID Z-2525-2026 · Official record ↗
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
Company / brand: TMJ Solutions recalls
Official ID Z-2524-2026 · Official record ↗
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe…
Company / brand: Philips North America recalls
Official ID Z-2523-2026 · Official record ↗
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe…
Company / brand: Philips North America recalls
Official ID Z-2522-2026 · Official record ↗
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engage…
Company / brand: Intuitive Surgical recalls
Official ID Z-2521-2026 · Official record ↗
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…
Company / brand: Medline Industries recalls
Official ID Z-2455-2026 · Official record ↗
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…
Company / brand: Medline Industries recalls
Official ID Z-2454-2026 · Official record ↗
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…
Company / brand: Medline Industries recalls
Official ID Z-2453-2026 · Official record ↗
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…
Company / brand: Medline Industries recalls
Official ID Z-2452-2026 · Official record ↗
Undeclared allergen, sesame.
Company / brand: Boichik Bagels recalls
Official ID H-1133-2026 · Official record ↗
Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
Company / brand: Boichik Bagels recalls
Official ID H-1132-2026 · Official record ↗
Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
Company / brand: Boichik Bagels recalls
Official ID H-1131-2026 · Official record ↗
Undeclared allergens: Milk and Soy
Company / brand: CERELES EN GENERAL SAS recalls
Official ID H-1124-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1123-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1122-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1121-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1120-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1119-2026 · Official record ↗
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Company / brand: George J Howe Company recalls
Official ID H-1118-2026 · Official record ↗
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1117-2026 · Official record ↗
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1116-2026 · Official record ↗
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1115-2026 · Official record ↗
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1114-2026 · Official record ↗
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1113-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.