On October 29, 2026, the Food and Drug Administration announced a recall involving the StatStrip Glucose Hospital Meter System due to potential risks of assigning glucose results to the wrong patient. Nova Biomedical…
Vitality Works Inc. of Albuquerque, New Mexico, is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules due to potential contamination with Salmonella, according to the…
The Food and Drug Administration (FDA) is classifying the software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer into class II (special controls) effective October 30…
On October 30, 2026, the Food and Drug Administration (FDA) announced the classification of radiology software for referral of findings related to fibrotic lung disease into class II (special controls). This…
On October 30, 2026, the Food and Drug Administration (FDA) issued a final order classifying the spinal imaging system for neuraxial procedures into class II (special controls). The FDA determined that this…
The Food and Drug Administration (FDA) is classifying the over-the-counter device to assess risk of sleep apnea into class II (special controls) effective October 30, 2026. According to the FDA, this classification…
American Health Packaging is recalling Metoclopramide Tablets, USP, 5 mg, due to the presence of foreign tablets or capsules. The recall, classified as Class II, began on October 6, 2026, and is ongoing, affecting…
On September 29, 2026, Teva Pharmaceuticals USA, Inc initiated a recall of Metoclopramide Tablets, USP, 5 mg, due to the presence of foreign tablets or capsules. The recall, classified as Class II, may cause temporary…
On October 21, 2026, the Food and Drug Administration announced a Class I recall of medical devices from Instrumentation Laboratory. The recall, which began on September 3, 2026, affects the HemoslL AcuStar…
SLR Food Distribution Inc. of Hicksville, New York, is recalling Wise Wife Brand Ground Cinnamon due to potential contamination with elevated levels of lead, according to a release published on October 29, 2026. The…
On October 28, 2026, the Food and Drug Administration (FDA) announced that Medline has issued an Urgent Medical Device Field Safety Notice regarding the discontinuation and market exit of all Medline Brand beds and…
The U.S. Food and Drug Administration announced the launch of the Neuroscience Advancement and Innovation Nexus (NAIN) on October 22, 2026. This new program aims to advance the science, tools, and regulatory approaches…
On October 20, 2026, B. Braun notified customers of a recall for the Streamline Bloodline Set for Dialog+, citing a potentially high-risk device issue. The Food and Drug Administration (FDA) issued an Early Alert on…
On October 27, 2026, Taylor Farms of Dallas, Texas announced a recall of the H-E-B Backyard BBQ Chop Salad kit due to the potential undeclared soy and tree nuts (almonds). The company stated that individuals with…
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