These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Beckman Coulter recalled its UniCel DxH 800 COULTER Cellular Analysis System on August 13, 2025. This recall affects devices that may produce inaccurately high hemoglobin results in patients with high white blood cell counts. The recall impacts worldwide distribution including numerous states in the U.S. and many countries.
Philips recalled 210 Brilliance iCT CT systems on August 13, 2025. A misalignment in the ball screw may cause the patient support table to descend unexpectedly. Patients and healthcare providers must stop using the device immediately.
Sandoz, Inc. recalled 1,680 bottles of Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension on August 13, 2025. The recall stems from temperature abuse that may compromise the product's efficacy. Consumers should stop using the product immediately and contact their healthcare provider or Sandoz for guidance.
Fresh & Ready Foods LLC recalled 233 units of Spanish Club Ciabatta sandwiches on August 13, 2025. The recall stems from undeclared allergens, specifically wheat and milk, posing a high risk to consumers. The products were available at 15 corporate locations across California.
Fresh & Ready Foods LLC recalled 233 units of Piccolo Pranzo Box sandwiches on August 13, 2025. The recall follows the discovery of undeclared allergens, specifically wheat and milk, posing a serious risk to consumers. The recalled products were distributed to 15 locations across California.
Philips recalled three Ingenuity CT Family systems on August 13, 2025, due to a hazard that could lead to sudden descent. The issue stems from a ball screw misalignment affecting the patient support table. Users should stop using the devices immediately and follow recall instructions.
Philips recalled 73 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728240, 728246, and 728256 distributed worldwide. This recall includes systems sold across the US and several countries globally.
Philips recalled 181 CT scanner units on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728235, 728231, and 728317 distributed worldwide. Healthcare providers and patients must stop using these devices immediately to ensure safety.
Philips recalled 24 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The issue stems from a misalignment in a component after replacement. Health providers must stop using these devices immediately.
Beckman Coulter recalled the UniCel DxH 600 Cellular Analysis System on August 13, 2025. The devices may produce erroneously high hemoglobin results in patients with elevated white blood cell counts. This recall affects medical facilities worldwide, including the United States.
Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System on August 13, 2025. Erroneously high hemoglobin results may occur in patients with elevated white blood cell counts. Healthcare providers and patients must stop using the device immediately.
Beckman Coulter recalled the UniCel DxH 900 COULTER Cellular Analysis System on August 13, 2025, due to erroneous high hemoglobin results. The devices may misreport hemoglobin levels on samples with elevated white blood cell counts. This recall affects devices distributed worldwide, including the U.S.
Change Healthcare recalled 12 programs of its Radiology Solutions software version 14.2.2 on August 13, 2025. A software issue may prevent radiology reports from displaying fully. Healthcare providers and patients must stop using the software immediately.
Siemens Medical Solutions USA recalled 20 Artis Pheno. Image-Intensified Fluoroscopic X-Ray Systems due to limited system movements after startup. The recall, announced on August 12, 2025, affects devices distributed nationwide across several states.
Wegmans Food Markets recalled 4,884 units of Caramel Apple Pecan Topped Brie Cheese on August 12, 2025. The cheese may be contaminated with Listeria monocytogenes, a serious pathogen. Consumers should not consume this product and seek a refund.
Wegmans Food Markets recalled 4,884 units of Medium Camembert Soft Ripened Cheese on August 12, 2025. The product may be contaminated with Listeria monocytogenes, posing a serious health risk. Consumers should not eat the cheese and should contact the company for refunds.
Max Mobility recalled 8,413 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection poses a risk of losing control of the wheelchair, leading to potential injuries. Healthcare providers should stop using the device immediately and follow recall instructions.
Viona Pharmaceuticals recalled 3,960 bottles of Tavaborole Topical Solution on August 12, 2025. The product may show discoloration, posing health risks to consumers. This recall affects topical solutions distributed nationwide in the USA.
Max Mobility recalled 25,389 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection can lead to loss of control, posing injury risks. Users must stop using the device immediately and follow recall instructions.
Baker's Authority recalled 70 units of Graham Cracker Meal on August 12, 2025, due to undeclared allergens. The product lacks proper labeling for wheat and soy, posing a serious health risk to allergic consumers. These items were distributed across multiple states including NY, CA, and TX.