Recall archive
31,892 recalls · page 204 of 1329
Consumer productsReported Nov 14, 2024
New Cosmos USA Recalls Combination Natural Gas and Carbon Monoxide Alarms Due to Failure to Alert Consumers to the…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.New Cosmos USA Inc.
CPSC
Consumer productsReported Nov 14, 2024
Petidoux Recalls Children's Pajamas Due to Burn Hazard; Violation of Federal Flammability Regulations for Children's…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Petidoux
CPSC
Consumer productsReported Nov 14, 2024
Stokke Recalls YOYO³ Strollers Due to Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stokke LLC
CPSC
Consumer productsReported Nov 14, 2024
Outdoor Essentials Recalls Cultivar Planter Boxes Due to Injury Hazard; Sold Exclusively at Tractor Supply Company
High riskUsing this product could cause serious injury, illness or death — stop using it now.UFP Saginaw LLC, dba Outdoor Essentials
CPSC
Consumer productsReported Nov 14, 2024
woom Bikes USA Recalls Children's OFF, OFF AIR and ORIGINAL 6 Bicycles Due to Fall and Crash Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.woom Bike USA LLC
CPSC
Reported Nov 13, 2024
Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological sponges for use in the protection of neural tissue during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Surgical Company, LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Hillrom Welch Allyn HScribe Holter System; ambulatory monitoring
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2024
The Access Cortisol assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
intelliPATH Universal HRP Detection Kit, REF: IPK5011G80, containing DAB Buffer, Catalog Number: IPBF5009G20; ONCORE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Cartesion Prime, Digital PET-CT, Model: PCD-1000A/3D.004, PCD-1000A/3D, is a diagnostic imaging system that combines…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Kirkland Signature Unsalted Sweet Cream Butter, Net Wt 16 oz (1 lb) 453g, Four 4 oz (113g) sticks UPC 96619-38496.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Continental Dairy Facilities Southwest LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2024
MEGA 7.5Fr. 40cc Intra-Aortic Balloon with Accessories, Model Number 0684-00- 0295-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Adult Cough and Chest Congestion (Dextromethorphan HBr USP 20 mg, Guaifenesin USP 400mg), packaged in 4 oz bottles…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Denison Pharmaceuticals, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
DeRoyal C-SECTION TRACEPACK, REF 89-9338-06
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Direct Rx
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, Diameter / 14 Gauge, containing 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elekta Instrument AB
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos, danes ellotes, danes cuernos,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EM Tortillas, LLC
FDA (openFDA food enforcement)
Reported Nov 13, 2024
Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FDC Limited
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hammond's Candies Since 1920 II, LLC
FDA (openFDA food enforcement)
Reported Nov 13, 2024
iotaSOFT Plus Drive Unit, REF IM-05. The iotaSOFT Insertion System is intended to aid the surgeon in placement of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Iotamotion Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
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