Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
A New Life Herbs recalled 48 bags of Organic Ginger Root Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume the product and seek a refund.
A New Life Herbs recalled 275 bottles of Pain Away Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume this product and seek refunds.
A New Life Herbs, LLC recalled 23 bottles of its Baby Allergy Herbal Supplement on November 20, 2025. The recall follows unapproved drug claims and absence of a Supplement Facts label on the product. Consumers should not consume the supplement and should seek refunds immediately.
Sonex recalled two aluminum pots on November 19, 2025, due to leachable lead levels of 0.323mg/L. The recall affects products distributed in New York. Consumers must stop using the product and seek refunds or replacements.
Vortex Surgical recalled 221 units of the 25ga Illuminated Flex-Tip Laser Probe on November 19, 2025. The product does not pass through a 25ga cannula smoothly, which poses a high hazard risk. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
Steris recalled 22 AMSCO 7053HP Washer/Disinfectors on November 19, 2025, due to a risk of electrical arcing. The issue arises from a wire connected to the electrical box that may shift from its intended position. Users must stop using the device immediately and follow recall instructions.
Steris recalled the AMSCO 7052HP Washer/Disinfector on November 19, 2025, after reports of electrical arcing. The issue results from a wire potentially shifting out of position, posing a fire risk. No injuries or shocks have been reported.
GUSTO GROUP recalled 7 cases of DPA161 Shrimp Paste on November 19, 2025. Testing revealed elevated lead levels in the product. Consumers in Iowa and New Jersey should not consume this product.
GUSTO GROUP, INC. recalled 7 cases of Shrimp Paste (Klong Kone) 'M' due to high lead levels. The recall affects products distributed in Iowa and New Jersey. Consumers should not consume the product and seek refunds immediately.
New Way Import Inc recalled preserved mustard on November 19, 2025, due to undeclared wheat allergens. The product, sold in predominantly green packaging with black Chinese lettering, poses a high risk to consumers with wheat allergies. Approximately 55 cases of the product were distributed to 23 retail locations in California.
JR Simplot Company recalled 7,053 cases of Traditional Reduced Sodium Tater Gems on November 18, 2025. The recall is due to plastic fragments embedded in the product, posing a choking hazard. Consumers in 15 states are advised not to consume the affected items.
Glenmark Pharmaceuticals recalled 672 bottles of Nebivolol Tablets on November 18, 2025, due to cross-contamination. The 20 mg tablets, prescribed for hypertension, may pose health risks. Consumers should stop using the product and seek guidance from healthcare providers.
Karabetian Import and Distribution recalled 338 boxes of Zimi Puff Pastry on November 18, 2025. The recall was initiated due to the presence of partially hydrogenated oils, which are not permitted in foods exported to the U.S. Consumers should not consume the product and seek a refund or replacement.
Karabetian Import and Distribution recalled 338 boxes of Zimi Kunefe on November 18, 2025, due to partially hydrogenated oils. The recall affects frozen dessert products distributed in nine states including California and Texas.
AGFA Healthcare recalled 35 Digital Radiography X-Ray systems on November 18, 2025, due to a risk of exceeding safe radiation levels. The recall affects systems distributed nationwide in the U.S. Users must stop using the device immediately and follow manufacturer instructions.
Sheathing Technologies recalled 12 units of its ultrasound probe covers on November 17, 2025, due to potential contamination risks. The non-sterile vaginal and rectal covers may have defects that pose an infection risk during use. Consumers should stop using the product immediately and follow the manufacturer's instructions.
Sophysa recalled 105 units of the Pressio 2 ICP Monitoring System on November 17, 2025, after receiving customer complaints regarding unexpected rebooting. This defect poses a high risk for patients relying on the device for monitoring intracranial pressure. Users should stop using the device immediately and follow the manufacturer's instructions.
ETAC A/S recalled 25 units of the Molift 4-point sling bars on November 17, 2025, due to a defect that can lead to improper functionality. The issue stems from a bolt that may break during assembly and load testing, posing a high risk during use. This recall affects products distributed worldwide, including the United States and several European countries.
ETAC A/S recalled 64 units of Molift 2-point sling bars on November 17, 2025. A defect in the mounting bolt can lead to failure during use. This poses serious risks for users relying on the device for mobility assistance.
Molift recalled 71 Mover 300 mobile hoists on November 17, 2025, due to a potential bolt failure. The defect can lead to limited mobility, posing a high risk to users. Affected models include M1501, M1502, M1504, among others.