State
20,304 recalls have nationwide distribution and so reach California. 0 additional recalls listed California specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect California consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Natus Medical is recalling 3,336 units of the EDS 3 CSF External Drainage System nationwide because incomplete bioburden testing cannot guarantee sterility. No illnesses have been reported, but non-sterile devices pose infection risk.
Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.
Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.
Merit Medical Systems is recalling specific lots of microcatheter and infusion system devices because their sterility cannot be guaranteed. The devices were distributed worldwide including multiple US states and international locations.
Medtronic is recalling Protege GPS Self-Expanding Peripheral Stent Systems due to seal defects in product packaging that could compromise sterility. Affected lot B644679 had national distribution.
Mack Trucks is recalling certain 2024 Anthem and Pinnacle vehicles due to a software error that may disable the electronic stability control system, increasing crash risk. Dealers will reprogram the control unit at no cost.
Philips recalled Trilogy Evo respiratory devices for missing contraindications in labeling. Devices lack warnings against use in pediatric patients under 10 kg and certain therapy modes, risking barotrauma and respiratory complications.
Spring Valley Biotin & Collagen Liquid is being recalled due to potential mold contamination. Approximately 24,324 units were distributed nationwide; consumers should stop using affected products.
Azurity Pharmaceuticals recalls Eprontia (topiramate) oral solution nationwide because routine stability testing found an out-of-specification impurity. The chemical defect raised concerns about the drug's purity and patient safety.
Abiomed has disabled four features in the Impella Connect software portal because the FDA has not evaluated them for safety and effectiveness.
Encore Medical has voluntarily recalled a patella implant component (REF 130-03-738) due to mislabeling. The recall involves 2 units distributed nationwide.
Encore Medical is recalling 17 Reverse Shoulder System e+ surgical implants (Lot 381P1167) due to mislabeling. Affected units were distributed nationwide to multiple states.
Keystone Industries is recalling 336 units of KeySplint Hard Clear due to incorrect Instructions for Use packaged with the product. Affected units received KeySplint Soft instructions instead.
Kia is recalling 2018-2021 Stinger vehicles due to a fuel control valve defect that can cause loss of drive power and increased crash risk. Dealers will update engine software and replace the fuel pump as needed.
Certain 2021-2023 Thomas Built school buses may lose critical driving functions due to automatic electrical switch failure. Dealers will remove the faulty switch at no cost.
Toyota is recalling 2023 Tundra and Tundra Hybrid vehicles with spray-on bed liners due to an incorrect load carrying capacity label. The label overstates capacity, risking vehicle overload and crashes.
Certain 2025 Freightliner and Western Star commercial trucks may have defective front axle tie rods that can fail and cause loss of steering control. Owners should contact DTNA at 800-745-8000 for free replacement.
Chrysler is recalling certain 2022 Jeep Gladiator vehicles due to a defective transmission park pawl that may not properly engage, potentially causing vehicle rollaway.
The left rear seat back in certain 2023 Dodge Charger vehicles may not lock in the upright position. This creates a risk of injury in a crash.
Chrysler is recalling certain 2021 Jeep Wrangler and Gladiator vehicles due to a powertrain control module software defect that may cause engine stall, resulting in loss of drive power and increased crash risk.
Certain 2021 Jeep Gladiator vehicles have a radio software error that may prevent the rearview camera image from displaying. This reduces rear visibility and increases the risk of backing collisions.
The left rear seat back in certain 2023 Dodge Challengers may not lock in the upright position, increasing the risk of injury in a crash. Dealers will inspect and adjust the seat latch free of charge.
Rivian is recalling certain 2022 R1T and R1S vehicles because front seat belt anchors may be inadequately attached to the B-pillar, potentially preventing proper restraint during a crash.
General Motors is recalling 2024 Chevrolet Malibu vehicles that may have an incorrect owner's manual. The wrong manual could contain inaccurate vehicle safety information.
Lucid is recalling certain 2022 and 2023 Air vehicles due to a software fault that could disconnect the high voltage system while driving, causing loss of drive power and increasing crash risk. A free over-the-air software update is available.