Recalls distributed in Massachusetts
These notices name Massachusetts 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.
4,249 stored notices name Massachusetts, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.
Reported May 21, 2014
Recalled product is a component of the Newport Medical Instruments e360 Ventilator: single board computer, part number…
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 May 21, 2014
Syngo Dynamics v9.5 system. A Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 14, 2014
Variant II beta-thalassemia Short Program Model Numbers 270-2103 (250 tests) and 270-2154 (500 tests), Bio-Rad…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 14, 2014
Bissinger's Dark Chocolate Bunny Ears, 1 oz, individually wrapped in clear plastic with an ingredient card insert and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Karl Bissinger LLC
FDA (openFDA food enforcement)
Reported May 14, 2014
Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mar Cor Purification
FDA (openFDA device enforcement)
Reported May 14, 2014
SpineFrontier S-Lift Lock Shaft Inserter, an instrument used with S-LIFT Intervertebral Body Fusion Device in spinal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SpineFrontier, Inc.
FDA (openFDA device enforcement)
Reported May 14, 2014
Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 14, 2014
Scale label printed with "EASTER BREAD NET WT 17oz (1.06lb)" UPC 0 77890 32431 8, packaged in clear plastic bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported May 7, 2014
ExacTrac 6.0 is a patient positioning and monitoring system. Model/catalogue numbers: 20833B EXACTRAC 6.0 IR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported May 7, 2014
HexaPOD evo RT Couchtop. To support and aid in positioning a patient during radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 7, 2014
Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 7, 2014
CAPIO, Monodeck, Violet Monofilament Polydioxanone Suture, 1 x 48 inches (122cm) Absorbable Surgical Suture, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Molecular
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Jolly Time Microwave popcorn, Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Pop Corn Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Creative Snacks Co. Dried Apricots (10.5 oz Rigid Plastic Cup, and 7 oz Clear Plastic Bag), Distributed by: Creative…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Creative Snacks Co., LLC
FDA (openFDA food enforcement)
Reported Apr 30, 2014
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
RaySearch Ray Station Radiation Therapy Treatment Planning System, Stand-alone software. Versions 2.0, 2.5, 3.0, 3.5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Brainlab, Spine & Trauma 3D 2.0, Navigation Software. An intraoperative image-guided localization system to enable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Luna Chocolate Chunk; Whole Nutrition Bar for Women; 15 count box. Clif Bar & Company, Emeryville, CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clif Bar And Company
FDA (openFDA food enforcement)
Reported Apr 23, 2014
OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with foil cap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Magno Humphries Laboratories, Inc.
FDA (openFDA food 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.