Recall archive
31,892 recalls · page 212 of 1329
Reported Oct 16, 2024
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with StealthStation Spine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
FDA (openFDA device enforcement)
Reported Oct 16, 2024
FastPack TSH Calibrator Kit, REF: 25000024, For use in conjunction with the FastPack IP TSH Immunoassay and FastPack IP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qualigen Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to assist in the planning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quantum Surgical Sas
FDA (openFDA device enforcement)
Reported Oct 16, 2024
STASKA Pharmaceuticals Inc. recalls STASKA Pharmaceuticals Ascorbic Acid Solution for Injection due to Device & Drug Safety – Presence of glass particulates
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.STASKA Pharmaceuticals Inc.
FDA (recalls & safety alerts)
Reported Oct 16, 2024
The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker(s)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zyno Medical LLC
FDA (openFDA device enforcement)
Reported Oct 11, 2024
Enoki King Mushroom Farm recalls Enoki King Enoki Mushroom 5.3 oz due to Potential Listeria monocytogenes contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Enoki King Mushroom Farm
FDA (recalls & safety alerts)
Reported Oct 11, 2024
Reser’s Fine Foods recalls Bistro 28, Don Pancho Meal kits containing chicken due to Potential Listeria monocytogenes contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Reser’s Fine Foods
FDA (recalls & safety alerts)
Reported Oct 11, 2024
Tipical Latin Food Corp. recalls Los Andes Foods Cachapa de Maiz sweet corn pancakes due to Potential or Undeclared Allergen - Wheat
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Tipical Latin Food Corp.
FDA (recalls & safety alerts)
Reported Oct 11, 2024
Wismettac Asian Foods, Inc. recalls Shirakiku Korean Seasoned Seaweed due to Potential or Undeclared Allergen - Sesame
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Wismettac Asian Foods, Inc.
FDA (recalls & safety alerts)
Consumer productsReported Oct 10, 2024
Fisher-Price Recalls More than 2 Million Snuga Infant Swings Due to Suffocation Hazard After 5 Deaths Reported
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fisher-Price
CPSC
Consumer productsReported Oct 10, 2024
Homewerks Worldwide Recalls Allen + Roth Lighted Bathroom Mirrors Due to Injury and Laceration Hazards; Sold…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Homewerks Worldwide LLC
CPSC
Consumer productsReported Oct 10, 2024
NPW Group Recalls Halloween Projector Flashlights Due to Fire and Burn Hazards; Sold Exclusively at Target
High riskUsing this product could cause serious injury, illness or death — stop using it now.NPW Group
CPSC
Consumer productsReported Oct 10, 2024
Gimars Playpens Recalled Due to Entrapment and Suffocation Hazards; Violation of Federal Regulations for Play Yards;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shenzhen Jingdu Technology Co. Ltd.
CPSC
Consumer productsReported Oct 10, 2024
Reyhee Group and Jingling International Recall Droyd Fury Youth All-Terrain Vehicles (ATVs) Due to Laceration Hazard;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yongkang Ruihe Metal Products Co. Ltd.
CPSC
Consumer productsReported Oct 10, 2024
Reyhee Group Recalls Droyd Multi-Purpose Helmets Due to Risk of Head Injury; Violation of Federal Regulations for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yongkang Xinhao Industry and Trade Co. Ltd.
CPSC
Reported Oct 9, 2024
Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Accelerator Applications USA, Inc.
FDA (openFDA drug enforcement)
Reported Oct 9, 2024
DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Oct 9, 2024
BD FACSDuet Premium Sample Preparation System, REF: 666340, 666339; and BD FACSDuet Sample Preparation System (Base),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Bio Sciences
FDA (openFDA device enforcement)
Reported Oct 9, 2024
BIG BOTTOM MILK COMPANY, CHOCOLATE MILK GRADE A, 1 US Gallon (3.79 liters), Big Bottom Milk Company 221 Hogan Rd,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Big Bottom Milk Company
2 more products in this recall
FDA (openFDA food enforcement)
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