2,715 recalls tagged with “immediate action”.
PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Vegetable Tray Cucumbers on May 20, 2025. The recall follows contamination with Salmonella, posing a high health risk. The affected products were distributed in Virginia, New York, Pennsylvania, and New Jersey.
PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of sliced cucumbers on May 20, 2025. The product may contain Salmonella, a serious health risk. Consumers should not eat the product and seek a refund immediately.
PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of sliced cucumbers on May 20, 2025. The product is contaminated with Salmonella, posing a serious health risk. The recall affects consumers in Virginia, New York, Pennsylvania, and New Jersey.
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 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.
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.
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.
Ventura Foods recalled over 17,000 cases of creamy peanut butter on April 30, 2025. The recall follows reports of foreign blue plastic found in the product. Consumers should not consume the affected products and are urged to seek refunds.
Ventura Foods recalled 929 cases of peanut butter and grape jelly on April 30, 2025. The company found pieces of blue plastic in the product during production. Consumers should not consume this product and can seek refunds or replacements.
Ventura Foods recalled 379 cases of its peanut butter and strawberry jam duo on April 30, 2025. Pieces of blue plastic were found in the product during production. Consumers should not eat the product and should seek a refund.
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.
Sanders Candy Factory recalled 5,020 pounds of bulk almonds on March 25, 2025. Elevated levels of aflatoxin prompted the recall. The product was distributed to one customer and not sold to consumers.
ESAOTE recalled 5 Endocavity Ultrasonic Probe E 3-12 units sold in the United States to healthcare providers in NC and TX. A potential weakness in the probe body could cause liquid to leak from the terminal part of the casing near the cable. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.
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.
Olympus Corporation of the Americas recalled 633 units of the Cystoscope Outer Sheath, Model WA22810A on September 13, 2024. The recall occurred due to potential device damage when used with a GreenLight Laser for BPH therapy. Healthcare providers and patients must stop using the device immediately and follow recall instructions.