Agency
The FDA regulates food, drugs, biologics, medical devices, and tobacco. We aggregate Class I, II, and III enforcement actions across its three recall streams.
The FDA is the single biggest source of US product recalls by volume. Its enforcement workload splits into three streams — Foods (everything from infant formula to leafy greens to nutritional supplements), Drugs (prescription medicines, over-the-counter products, and active pharmaceutical ingredients), and Medical Devices (everything from implants to home blood-pressure monitors). The Recall Desk ingests all three from the openFDA enforcement endpoint every six hours.
FDA classifies every recall as Class I, II, or III. Class I means there is a reasonable probability that using the product will cause serious health consequences or death — these are the recalls you should treat as urgent. Class II means the product may cause temporary or medically reversible harm. Class III means the product is unlikely to cause adverse health consequences but still violates FDA rules. We map these classifications into our 1–5 severity score using the rubric on the methodology page.
Medical-device recalls are the highest-volume stream by far — software-update letters, calibration corrections, and IFU updates all show up in enforcement reports alongside genuine hazard recalls. We try to surface the severe ones first, but when in doubt, click through to the FDA notice itself for the clinical detail.
Meijer is recalling Fresh From Meijer Tomato Caprese Salad due to potential Listeria monocytogenes contamination. The product was distributed to stores across six states.
EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.
Cordis is recalling an emboli capture guidewire system due to potential separation of components during medical procedures. The separation could cause procedural delays, unplanned interventions, or stroke.
Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.
Revolution Farms Zesty Southwest salad kits are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.
Revolution Farms is recalling Green Sweet Crisp and Sweet Crisp Deli Leaf products from Michigan, Ohio, and Wisconsin due to potential Listeria monocytogenes contamination. Consumers should not eat and should discard affected products.
Meijer Inc. is recalling Fresh From Meijer Chicken Cobb Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in six states.
Revolution Farms romaine lettuce products distributed in Michigan, Ohio, and Wisconsin are recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should discard them.
Revolution Farms is recalling Traverse City Cherry 6-ounce salad kits due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.
Revolution Farms Sesame Ginger Crunch 6oz salad kits (UPC 856791008233, 'Sell By 3/23/23') are recalled due to potential Listeria monocytogenes contamination. Affected units were distributed in Michigan, Ohio, and Wisconsin.
Meijer Inc. is recalling Fresh From Meijer Chicken Caesar Salads (6.4 oz and 10 oz sizes) due to potential Listeria monocytogenes contamination. Products were distributed to Meijer stores in six states: Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
Cordis US Corp is recalling the ANGIOGUARD RX / XP Emboli Capture Guidewire System because the device may separate during procedures, risking stroke or requiring emergency intervention.
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.
Fresh From Meijer Shareable Garden Salad 11.5 oz is being recalled due to potential Listeria monocytogenes contamination. The recall affects salads distributed to Meijer stores across six states with a sell-by date of 3/31/2023.
ANGIOGUARD RX/XP emboli capture guidewire systems may separate from their delivery sheaths during interventional procedures, potentially causing stroke. Cordis is recalling 56 units distributed worldwide.
Cordis US Corp's ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled by the FDA (Class I) because the delivery system and capture sheath may separate during medical procedures, potentially requiring emergency intervention.
Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.
The FDA has recalled the ANGIOGUARD RX/XP Emboli Capture Guidewire System because the delivery system and capture sheath could separate during use, potentially causing stroke or requiring emergency surgery.
The ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled because the delivery system and capture sheath may separate during procedures, potentially causing stroke or requiring emergency surgical intervention.
Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.
Kanro Non-Sugar Tea House 40g has been recalled because coconut allergen is not listed in the product ingredients. Consumers with coconut allergies should not consume this product.
Borris Brothers is recalling Smoked Wahoo Dip due to undeclared Yellow #5 (tartrazine), an allergen that may affect consumers with sensitivity. The recall affects 112 containers distributed in Florida.
Daisho crab miso soup is being recalled because the product contains shrimp but the label warns only for crab, posing a risk to consumers with shrimp allergies. Products were distributed across multiple US states and Canada.
Borris Brothers voluntarily recalls 55 containers of Smoked Swordfish Dip (8oz) distributed in Florida due to undeclared Yellow #5, a color additive that can trigger reactions in sensitive individuals.
Daiso California Warehouse is recalling Fujiya Country Ma'am Vanilla & Cocoa wafers because they contain peanut (sheanut) that is not declared on the label. Consumers with peanut allergies should not consume this product.