280 recalls tagged with “replacement available”.
Pacific Coast Fresh Co. recalled 760 King Harvest Jalapeno Hummus containers distributed in Oregon and Washington. Aluminum pieces were found as a foreign material in the product. Consumers should not consume this hummus and should contact the company for refund or replacement.
Pacific Coast Fresh CO is recalling 239 containers of King Harvest Spinach Hummus sold in Oregon and Washington. Each 10-ounce tub bears UPC 025726311087 and Best By date 2/27/2026. Stop using the product immediately due to aluminum fragments and call Pacific Coast Fresh CO by telephone for refund or replacement.
Pacific Coast Fresh CO recalls 348 10-ounce King Harvest Sundried Tomato Hummus containers sold in Oregon and Washington after aluminum pieces were found. The hazard is foreign material aluminum pieces in the hummus. Consumers should not consume the product and should contact Pacific Coast Fresh CO by telephone for refund or replacement.
Imu-Tek Animal Health recalled 1,003 bottles of Colostrum-5 sold through various retailers in 30 states after determining the product may be under-processed. The under-processing could render the product unsafe. Consumers should not consume the product and should contact Imu-Tek Animal Health for refund or replacement.
King Harvest Roasted Red Pepper Hummus, distributed in Oregon and Washington by Pacific Coast Fresh Co, is recalled. The recall cites foreign material aluminum pieces found in 10 oz and 17 oz tubs. Consumers should not eat the product and should contact Pacific Coast Fresh Co for a refund or replacement.
King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.
Siemens Healthcare Diagnostics recalled 21,291 Atellica CH A1c_E units distributed to laboratories nationwide and internationally in 2026. The recall addresses a depressed result bias when A1c_E is processed with RCRP on the same analyzer. Labs using separate analyzers are not impacted. Stop using the affected module immediately and follow manufacturer instructions. Contact Siemens or your lab’s F
Stryker Communications recalled 6,170 CHROMOPHARE Softlit Ring Surgical Light Systems distributed worldwide after confirming the ceiling cover weight may not be adequately supported. Hospitals should stop using the device immediately and follow recall instructions from the manufacturer. The recall is classified as Class II and is active as of February 23, 2026.
Mei Heong Yuen Garlic Flavor Roasted Peanuts, distributed by Super World Trading Inc., were recalled on Feb. 19, 2026. The products contain cyclamates, a banned sweetener. Consumers who purchased the product should not consume it and should contact the distributor for refund or replacement.
MEI HEONG YUEN Walnut Flavor Roasted Peanuts recalled in the United States by Super World Trading Inc. on Feb. 19, 2026. The product contains cyclamates, a banned sweetener. Consumers should not eat this product and should contact the distributor for refunds or replacements.
Mei Heong Yuen Tangerine Flavor Roasted Peanuts, distributed in the United States by Super World Trading Inc., are recalled across 595 cases under H-0641-2026. The product contains cyclamate, a banned sweetener. Consumers should stop consuming the product and contact the distributor for refunds or replacements.
AMO Puerto Rico Manufacturing recalls 361 TECNIS Eyhance IOL with TECNIS Simplicity Delivery System lenses sold nationwide through healthcare providers. The lenses may have a haptic that sticks to the optic, preventing unfolding as expected. Patients and clinicians should stop using the device immediately and follow recall instructions.
Radnostix recalled 2,699 gelatin capsule packs used with its Sodium Iodide I-131 kit, distributed nationwide in the United States and Puerto Rico. The capsules failed to meet tablet/capsule specifications. Healthcare providers and patients should stop using the product and contact Radnostix for guidance.
Abiomed has issued a Class I recall for 33,107 Purge Cassette units used with Impella pump sets worldwide due to purge leaks in Generation 1 cassettes. The leaks raise the risk of compromised device performance. Patients and healthcare providers should stop using the affected devices immediately and follow Abiomed's recall instructions.
Sunflour Bakery recalled 1 bag of Hamburger Bun, 18oz with six buns sold to a single Orange County retailer. The recall involves sesame seeds not declared on the label. Consumers should not eat the product and should contact Sunflour Bakery by email for refund or replacement.
Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs on February 18, 2026. Infusion sets may have dull or blunt needle tips that can be difficult to advance or break. Health facilities and patients should stop using the device immediately and follow the recall instructions.
Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.
Mentor Texas, LP recalled Artoura Breast Tissue Expanders worldwide after discovery of dull infusion needle tips. The issue may make it difficult to advance the infusion set or cause it to break. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Medline Industries recalled 420 Sterile Radiology Procedure Kits, Model DYNDH1491B, distributed nationwide in Minnesota after a potential breach in sterile pouch packaging. The defect may compromise product sterility. Stop using the kit immediately and contact Medline or your healthcare provider for instructions.
Mentor Texas, LP recalled Artoura Breast Tissue Expanders sold worldwide, including the United States. The infusion sets may contain a dull or blunt needle tip, which may be difficult to advance or break. Healthcare providers and patients should stop using the affected devices and await recall instructions by letter.