Recall archive
31,892 recalls · page 115 of 1329
Reported Oct 1, 2025
Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Consumer Product Partners, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 1, 2025
MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperVision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2025Updated Aug 26, 2026
Doan's Bakery recalls Doan's Bakery White Chocolate Coconut & Carrot Bundt Cakes due to Undeclared allergens, wheat and milk
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Doan's Bakery
FDA (recalls & safety alerts)
Reported Oct 1, 2025
PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, Inc., Yonkers, NY 10705, STORE IN A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Domino Foods Inc.
FDA (openFDA food enforcement)
Reported Oct 1, 2025
STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX SPI PDS+ BI VIO 14X14IN(36X36CM) USP1(M4)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extract Labs, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 1, 2025
Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Oct 1, 2025
GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gooder Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 1, 2025
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Granules Pharmaceuticals Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 1, 2025
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MEDLINE INDUSTRIES, LP - Northfield
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2025
READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medline Industries, LP
FDA (openFDA drug enforcement)
Reported Oct 1, 2025
1) Sunrise Creamery Dilly Pickle Monterey Jack Cheese with Dill Pickles, Net Wt. 6 oz., packaged individually in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Middlefield Original Cheese Cooperative
8 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 1, 2025
BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Oct 1, 2025
MMBAL pasteurized donor human milk (PDHM), 100 mL (3.38 fl. oz.), packaged in a BPA-free plastic bottle
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mothers' Milk Bank
FDA (openFDA food enforcement)
Reported Oct 1, 2025Updated Aug 26, 2026
New Age International Inc recalls Signature Enoki Mushrooms due to Product may be contaminated with Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.New Age International Inc.
FDA (recalls & safety alerts)
Reported Oct 1, 2025
Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortoma Ab
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2025
ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Private Label Skin Care Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 1, 2025
Sea Port Products Corp recalls Sea Port Raw Frozen Easy Peel White Shrimp Jumbo size 16/20 due to Product May Have Become Contaminated with Cesium-137 (Cs-137)
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Sea Port Products Corp.
FDA (recalls & safety alerts)
Reported Oct 1, 2025
Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
FDA (openFDA device enforcement)
Reported Oct 1, 2025
UDK ,Half Plum, 170 g, Container, 24, ambient
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sungal Inc.
FDA (openFDA food enforcement)
RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up