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 48,122 notices were distributed nationwide, so they reach Maine too — those are in the archive.
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Jul 30, 2014
RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2014
MK5 NX Controller--Wheelchair controller
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 30, 2014
Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2014
Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2014
ACL TOP (Base), automated coagulation laboratory instrument.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2014
There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NW Nutritional Foods LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 23, 2014
e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RGI Medical Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part Number 585006 contained in Alcon Assembly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, Ltd.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Ocean Spray¿ Greek Yogurt Covered Craisins¿ Dried Cranberries , 8 oz Resealable Pouch UPC: #23719
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ocean Spray Cranberries Inc.
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Ocean's Catch RTE Fresh Hand Picked Crabmeat , Net WT. 6 oz. plastic container Ingredients; Contains Jonah Crab Meat
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rome Packing Co., Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Ingenia 3.0T R5, magnetic resonance imaging system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2014
GE Healthcare, Compact Airway Modules E-CO, E-COV, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX. The Datex-Ohmeda S/5MT Compact…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jun 18, 2014
Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Jun 11, 2014
Greens+ Vegan Crisp Bars - Dark Chocolate Almond Blueberry in 1.4 oz packages.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orange Peel Enterprises, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Maine recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.