Recall archive
31,892 recalls · page 85 of 1329
Consumer productsReported Jan 8, 2026
Agrish Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zhongshan Lebo Medical Co., Ltd.
CPSC
Reported Jan 7, 2026
BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver-Visitec International, Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a cardboard box with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bendon Publishing
FDA (openFDA food enforcement)
Reported Jan 7, 2026
BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 213, LLC
FDA (openFDA drug enforcement)
Reported Jan 7, 2026Updated Aug 26, 2026
Carrot Top Kitchens recalls Carrot Top Kitchens Hummus Varieties due to Potential or Undeclared Allergen – Sesame
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Carrot Top Kitchens
FDA (recalls & safety alerts)
Reported Jan 7, 2026
Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferndale Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
Ondansetron Orally Disintegrating Tablets, USP, 4mg, 30 Tablets (3 blistercards each containing 10 tablets), Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Jan 7, 2026
ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Indian Cookware and Appliance LLC
FDA (openFDA food enforcement)
Reported Jan 7, 2026
Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novo Nordisk Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 7, 2026
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Jan 7, 2026Updated Aug 26, 2026
Primavera Nueva Inc. recalls Primavera Tamales due to Potential presence of Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Primavera Nueva Inc.
FDA (recalls & safety alerts)
Reported Jan 7, 2026
Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"L (2.2cm Tapered to 7.4cm x 30cm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sheathing Technologies Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
Material Processing Laser Products
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shenzhen Atomstack Technologies
FDA (openFDA device enforcement)
Reported Jan 7, 2026
Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is shelf stable, gold foil wrapping…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tom Bumble LLC
FDA (openFDA food enforcement)
Reported Jan 7, 2026
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vortex Surgical Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Zydus Pharmaceuticals (USA) Inc.
FDA (openFDA drug enforcement)
Reported Jan 5, 2026Updated Aug 26, 2026
Newway Import Inc. recalls Newway Import Preserved mustard in soybean oil due to Undeclared wheat
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Newway Import Inc.
FDA (recalls & safety alerts)
Reported Dec 31, 2025
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.A New Life Herbs, LLC
8 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 31, 2025
Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Dec 31, 2025
Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Numbers: 9903-20, 17188-04, 19762-03,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Dec 31, 2025
BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Dec 31, 2025
Zen Cleanse Blend herbal tea; .95 oz (27g) pouch; 18 pouches/box UPC: 819005011504
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bell Industries LLC
FDA (openFDA food enforcement)
Reported Dec 31, 2025
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Dec 31, 2025
Flexor Check-Flo Introducers and Sets, Reference Part Numbers: 1) KCFW-9.0-18/38-45-RB-ANL0-HC; 2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
2 more products in this recall
FDA (openFDA device enforcement)
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