State
72,820 recalls have nationwide distribution and so reach California. 13,244 additional recalls listed California specifically in their distribution scope.
Of the 13,244 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,842 (21%) are Severe.
Which agencies issued them
These figures cover only the 13,244 recalls whose distribution notice names California specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.
TooyBing is recalling its Wooden Bead Stacking Toys because the wooden beads pose a choking hazard to children under three years old.
Chrysler is recalling 81 2026 Jeep Grand Cherokee and Grand Cherokee L vehicles because a software issue may cause windshield wipers to fail, reducing visibility.
General Motors is recalling 2024-2025 Chevrolet Silverado 2500 and GMC Sierra 2500 trucks because incorrect tire pressure labels may cause underinflation and prevent low-pressure warnings.
SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.
CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.
Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.
COMMOWNER electric pressure washers (models HD14P-Z and HX18) are recalled due to shock and electrocution hazards from a missing built-in GFCI. No injuries reported; stop use and contact AZ Home Concept for a refund.
Qabefy twin mattresses sold on Amazon are recalled because they violate the federal flammability standard, posing a fire hazard. Consumers should stop using them and contact Qabefy for a refund.
Deli Jerry fuel containers sold on Walmart.com are recalled because their caps are not child-resistant, posing burn and poisoning risks to children. No injuries have been reported; consumers should stop using them and contact Deli OfficeSupplies for a refund.
Ritchey Design is recalling about 775 carbon bicycle forks because the alloy insert in the crown hole can come loose, letting an accessory fall onto the front wheel and cause a crash. No injuries have been reported.
Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.
AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.
Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.
AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.
AVID Medical, Inc. is recalling 5,168 Halyard convenience kits because they contain Medline Namic Angiographic Star Off Handle Manifolds that may have particulates in the fluid path.
AKKARCO LLC is voluntarily recalling Ashfiat Alharamain Energy Support (250ml/8fl. oz.) because it contains undeclared tadalafil.
Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.
United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.
Boston Scientific is recalling Radial Jaw 4 Jumbo Biopsy Forceps due to potential breach in the sterile barrier of device packaging. The recall affects 5,020 units in the US and 20,770 units outside the US.
Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.
Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.
Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.
GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.
BMW is recalling certain 2024-2026 X3 models because the steering spindle may be incorrectly attached to the steering column, increasing crash risks.