Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Cucumber Peeled Sliced on May 20, 2025. The product may be contaminated with Salmonella, posing a high health risk. Consumers should not consume the product and seek a refund or replacement immediately.
Chefs Warehouse recalled 15 lbs. of diced cucumbers on May 20, 2025, after discovering contamination with Salmonella. The recall includes products distributed in Maryland, Delaware, and Virginia. Consumers should not eat these cucumbers and should seek a refund or replacement immediately.
Chefs Warehouse recalled 98 cases of cucumbers on May 20, 2025, due to contamination with Salmonella. The recall affects cucumbers distributed in Maryland, Delaware, and Virginia. Consumers should not eat the product and can seek a refund.
Chefs Warehouse recalled 190 cases of Cucumber Select on May 20, 2025. The product poses a high risk of salmonella contamination. Consumers in Maryland, Delaware, and Virginia should not consume it.
Chefs Warehouse recalled 10 pounds of sliced cucumbers on May 20, 2025, due to Salmonella contamination. The affected products were distributed in Maryland, Delaware, and Virginia. Consumers should not consume these products and seek refunds immediately.
Chefs Warehouse recalled 5 lbs. of diced cucumber on May 20, 2025, due to Salmonella contamination. The product poses a high health risk to consumers. The recall affects states including Maryland, Delaware, and Virginia.
Medtronic recalled 1,440 Simplera Sensors on May 7, 2025. The device cap label may not adhere properly, compromising sterility and increasing infection risk. Patients should stop using the device immediately and contact their healthcare provider for instructions.
Turkana Food Inc. recalled 352 cases of Floria Dried Apricots on April 29, 2025. The recall follows the discovery that the product contains undeclared sulfites, posing a serious health risk. The affected products were distributed in multiple states across the U.S.
3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets on April 10, 2025. The recall addresses concerns about flow rates and inlet temperatures. Healthcare providers and patients must stop using the devices immediately.
World Perfumes recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic on February 13, 2025. The recall stems from reports of broken or leaking containers. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
MEDITECH recalled 148 units of its clinical calculator module on February 5, 2025 due to a malfunction that may result in data loss. Users may experience issues when entering multiple keys, causing data removal from the first field of screens or questionnaires. Medical Information Technology advises immediate cessation of use.
CorNeat Vision recalled the CorNeat EverPatch surgical matrix on October 16, 2024. The recall affects the product's labeling for prevention and management of wound dehiscence. Distribution spans across the U.S. and several countries.
Intuitive Surgical recalled 144 units of the da Vinci 5 Surgeon Console Column Motor Connector on August 21, 2024. Users reported a potential ergonomic lock issue that could delay or abort surgical procedures. Healthcare providers must stop using the devices immediately and follow the recall instructions.
Mothers' Milk Bank of Alabama recalled 25 bottles of pasteurized donor human milk on August 18, 2024. The recall follows concerns about potential physical contaminants. Consumers in Alabama should not consume this product and should seek refunds or replacements.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall affects devices distributed nationwide across six states due to potential failure of fusion system instruments. Patients and healthcare providers must stop using the devices immediately to avoid high-risk complications.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall follows reports of failure of fusion system instruments in the field. Healthcare providers and patients must stop using the device immediately.
NOXBOX recalled 1,667 Nitric Oxide Delivery Systems on July 19, 2023. The recall addresses high failure rates of the internal Sample Pump. Patients should stop using the device immediately and follow manufacturer instructions.
Foundation Medicine recalled 59 units of its FoundationOne CDx (F1CDx), RAL-0003 version 31.0 on November 8, 2022. The recall affects devices distributed in the U.S. and internationally due to missing important diagnostic information. Patients and healthcare providers must stop using the device immediately and follow manufacturer instructions.
Foundation Medicine recalled 18 units of the FoundationOne Liquid CDx (F1LCDx) on November 8, 2022. Reports sent to customers lacked the necessary companion diagnostic Claims Page. The issue affects customers across multiple U.S. states and in Japan and Singapore.
Philips recalled 1,721 EPIQ Ultrasound Systems on July 14, 2022. The ultrasound may unexpectedly reboot, damaging the transducer. Healthcare providers must stop using the device immediately.