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 27, 2019
Fructosamine Calibrator, FR2993 This product is intended for in vitro use in the calibration of the Randox Liquid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2019
AMSCO 3000 Series Washer/Disinfector Model # 3052
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 Mar 13, 2019
JANSAL VALLEY DUKKAH NET WT 2.5 oz. (71 G). The product is packaged in a circular tin can with a clear lid. UPC: 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Fruit Market dba Sid Wainer & Son
FDA (openFDA food enforcement)
Reported Mar 13, 2019
DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kingston Pharma LLC
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Mediterranean Stuffed Salmon packaged in plastic nonflexible containers
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
33 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Bar Company LLC Rxbar
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handpiece Headquarters
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jac Vandenberg Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 30, 2019
Perfusion Pack, Rx only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
FDA (openFDA device enforcement)
Reported Jan 28, 2019
Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Perdue Foods, Llc.
USDA FSIS
Reported Jan 23, 2019
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2019
StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2019
Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
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.