2,756 recalls tagged with “immediate action”.
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 278 bottles of Boswellia Herbal Supplement on November 20, 2025. The product has unapproved drug claims and lacks a Supplement Facts label. Consumers should stop using it immediately and seek a refund.
CareFusion 303 recalled 53,669 units of Automated Dispensing Cabinets on November 20, 2025. A firmware update caused drawer failures, leading to potential delays in accessing medications. This recall affects devices distributed worldwide, including all U.S. states and several countries.
Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.
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, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately and seek a refund.
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.
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.
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.
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.
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, 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.
Two Sonex aluminum pots sold in New York are recalled after tests found leachable lead at 0.323 mg/L. The recall is issued by Alanwar Food Corp. Consumers who own the pots should not use them for cooking and should contact Alanwar Food Corp. for refund or replacement information.
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.
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.
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.
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.
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.
Intuitive Surgical recalled 12 Da Vinci 5 surgical consoles on November 17, 2025. A software error may cause loss of user interface content on external monitors. Healthcare providers must stop using the devices immediately.
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.