State
20,199 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.
Sandford Family 6-Player Croquet Sets are recalled because paint on mallets, hoops, and winning posts contains lead and phthalates at levels that exceed federal bans. Lead and phthalates are toxic if ingested, especially for young children.
Oso & Me is recalling approximately 170 children's pajama sets that violate federal flammability regulations for sleepwear, posing a burn risk to children. No injuries have been reported.
Nutraceutical Corporation is recalling Heritage Store Hydrogen Peroxide Mouthwash because the packaging does not comply with child-resistant packaging requirements, posing a poisoning risk if swallowed by young children.
About 720 Liverpool Football Club children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn-injury risk. The pajamas were sold exclusively online from January 2022 through November 2023.
Vernier Science Education is recalling about 15,000 Go Direct Charge Stations because they can overheat and pose a burn hazard. The company has received two reports of overheating but no injuries have been reported.
SMART Technologies is recalling about 750 electric height-adjustable mobile stands for large interactive flat panel displays because wheelbase welds can bend or break during movement, causing the stands to tip over and create entrapment hazards.
Sustain Herbal Dietary Supplement is being recalled nationwide for containing undeclared tadalafil, a pharmaceutical ingredient. The product was marketed as a dietary supplement but contains an unapproved drug.
SCHWINNNG Herbal Dietary Supplement (Lot #2108, exp. 10/31/2024) is recalled nationwide because it contains undeclared nortadalafil, an active pharmaceutical ingredient used for male sexual enhancement. The FDA classified this as an unapproved drug.
Neptune's Fix Tianeptine Tablets are being recalled because the product contains tianeptine, a substance not approved by the FDA for any medical use. The recall affects 4,932 boxes distributed nationwide.
Neptune's Fix Tianeptine Elixir has been recalled because it contains tianeptine, an unapproved drug substance in the United States. Approximately 1 million bottles distributed nationwide are affected.
Arize Herbal Dietary Supplement contains an undeclared ingredient (nortadalafil), a pharmaceutical used in FDA-approved male sexual enhancement medications, making it an unapproved drug.
Insight Pharmaceuticals is recalling TING 1% Tolnaftate Athlete's Foot Spray due to benzene contamination. The recall affects approximately 59,644 cans distributed nationwide.
Neptune's Fix Tianeptine Elixir is recalled nationwide for containing tianeptine, an FDA-unapproved substance. The product was marketed without required FDA approval.
Olympus Corporation of the Americas is recalling ESG PK Cutting Forceps because the jaw may fracture during pre-procedure inspection or during the procedure, posing a potential injury risk.
Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.
Philips Azurion 7 imaging systems may experience power loss due to a potential short circuit in the power inverter, risking delays or termination of diagnostic and surgical procedures.
Bestco LLC is recalling Family Wellness Cherry Cough Drops nationwide due to potential glass and silicone particulates found during manufacturing. Consumers should stop use immediately.
MRP, LLC is recalling AQUABILITI AQUASTAT saline flush syringes because they may fail to meet USP standards for sodium chloride content after 12 months.
Mallinckrodt recalls TERLIVAZ (terlipressin) injection due to temperature excursion during shipping. A cGMP deviation may compromise drug stability.
Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.
Bestco LLC is recalling Meijer Cherry Cough Drops due to potential glass and silicone particulates found during manufacturing quality control inspections. Consumers should stop using the product immediately.
Ascend Laboratories recalls 71,244 sachets of Fosfomycin Tromethamine for failing quality specifications due to organic impurities. Patients with affected lots should consult their healthcare provider.
Synapse Cardiology PACS software versions 7.0–7.3.0 may calculate left ventricle mass incorrectly, potentially leading to misdiagnosis or wrong treatment plans. Thirteen units have been distributed in the US and Israel.
Philips has recalled certain Allura Xper interventional X-ray systems because the disk bay component may fail, potentially preventing system operation and imaging procedures.
Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.