Recalls distributed in Maine
These notices name Maine in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,801 stored notices name Maine, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Maine too — those are in the archive.
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Applied Medical Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Palmer and Company, dba Palmer Candy Co.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17 Net Wt: 10 lb (2-5lb bags)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dutch Valley Food Distributors Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Bariatric Bed - BAR600IVC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2017
SwishTapered Implant
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50Kg sizes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumedia Manufacturers, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Chord-X Chordal Sizer is designed to assist in determining the proper length of chordal replacement prostheses to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.On-X Life Technologies, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 The Halo One Thin-Walled Guiding Sheath is designed to perform…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Peripheral Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2017
Kettle Cuisine, LLC Recalls Chicken Soup Product Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kettle Cuisine Midco, LLC
USDA FSIS
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Angiodynamics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultroid Technologies, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.