2,756 recalls tagged with “immediate action”.
Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.
Boston Scientific is recalling 806 EndoVive Safety PEG Kits sold nationwide. The recall concerns BD ChloraPrep Triple Swabsticks with open or compromised seals that could compromise sterility or dry the antiseptic solution. Hospitals and patients should stop using the kits immediately and follow the manufacturer's recall instructions.
LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Italianway Import recalls 60 units of VERGANI 1944 MILANO Pandoro Classico Gluten Free after Teflon fragments were found in flaking molds. The recall covers 10 cases distributed in FL, MI and NJ. Consumers should not eat the product and must contact Italianway Import for refund or replacement by email.
SLADE GORTON & CO. recalled 190 cases of Wellsley Farms Atlantic Salmon on February 10, 2026. The product may contain Listeria monocytogenes, a serious health risk. Consumers should not consume this product and seek a refund or replacement.
Reflexion Medical recalled 12 RefleXion X1 Radiotherapy System RXM1000 units sold to hospitals and healthcare providers in the United States after a software defect could cause a 5mm or greater misalignment and underdose. The defect occurs during angular roll corrections followed by a repeat localization, and the roll corrections from the initial localization are not carried through to treatment.
1,134 units of Hortex Mieszanka 9 Spring Vegetable Mix are recalled in Illinois due to potential glass contamination. The recall involves LOT SoC1070925 and UPC 5900477018735. Consumers should stop using the product and contact Polski Ogrod Sp. z o.o. for refunds or replacements.
Airova recalled Aroeve air purifiers on February 9, 2026, due to fire and burn hazards. The recall affects model MK04 with serial numbers starting with 'BN' manufactured before July 2025. Consumers should stop using these air purifiers immediately and seek replacements.
H & N Group recalled 378 cases of frozen cooked shrimp on February 9, 2026. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds.
BD Kiestra recalled 82 units of its ReadA lab automation module on February 6, 2026, including 7 in the United States and 65 overseas. The issue arises after a system reboot when one or more modules become unreachable via the remote connectivity interface, potentially delaying plate retrieval from the incubator. The problem is intermittent and did not affect test results, assay performance, or var
Trividia Health recalled 12,067,458 TRUE METRIX blood glucose meters sold worldwide due to inadequate labeling. The manuals failed to emphasize that an E-5 error code could indicate a dangerously high blood glucose level. Users must stop using these devices immediately and contact their healthcare provider for further instructions.
Trividia Health recalled 1,001,534 TRUE METRIX PRO owner’s booklets used with glucose meters distributed worldwide through multiple retailers. The labeling fails to clearly warn that an E-5 error could indicate very high blood glucose and does not emphasize immediate actions. Consumers should stop using the device and follow manufacturer recall instructions by letter, contacting Trividia Health or
International Life Sciences issued an active recall of Artelon FLEXBAND TWIST augmentation devices. The devices were distributed worldwide, including nationwide in the United States. The recall concerns failures in bacterial endotoxin testing that could pose a infection risk; users should stop using the device and follow recall instructions from the manufacturer.
Trividia Health's TRUE METRIX GO blood glucose kits sold at Walgreens, CVS and other retailers are recalled worldwide. The labeling fails to clearly emphasize that an E-5 error could indicate very high blood glucose and require immediate action. Consumers should stop using the device and follow manufacturer guidance.
Trividia Health recalled 3,678,026 TRUE METRIX AIR owner’s booklets distributed worldwide through Walgreens, CVS and other retailers. The recall centers on labeling for the E-5 error code, which could indicate very high blood glucose and lacks clear, immediate action guidance. Consumers should stop using the device and await manufacturer instructions mailed to customers.
International Life Sciences recalled Artelon FlexBand Dynamic Matrix 31057 after endotoxin testing failures. The recall covers the augmentation device used in medical procedures. Patients and healthcare providers should stop using the device immediately and await manufacturer instructions.
Valley Springs Artesian Gold recalled 263,440 gallons of distilled water on February 6, 2026. The water was bottled under insanitary conditions, posing a health risk. Consumers in Illinois and Wisconsin should not consume the affected products.
International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.
Valley Springs recalled 379,868 units of bottled water on February 6, 2026. The recall affects multiple sizes and brands due to insanitary bottling conditions. Consumers should not consume the product and seek refunds or replacements.
Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.