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 Dec 26, 2012
MAYFIELD Composite Series Base Unit, Model A3101, a Swivel Adaptor (A3018) is an integral component of the Base Unit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 26, 2012
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ThyssenKrupp Access Corp.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
#122-A, Piazza Produce Clam Base, Net Weight 16 oz (1 lb) 454G Packed For: Piazza Produce, Indianapolis, IN 46268:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Williams West & Witt's Products Company
12 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2012
WANG Transbronchial Aspiration Needles Cat. No. MW-222, WANG Cytology Needles, Central or Peripheral Regions, 22 g x 13…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutaneous electrode is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC dba Uni-Patch
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Organic Gelato Chocolate Peanut Butter, 5 liter, contained in plastic packaging, manufactured by Fresca Foods, CO.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boulder Ice Cream
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2012
Blue Diamond Almond Breeze Almond milk Half Gallon (1.89 L) Paper Carton UPC: 4157005618
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HP Hood LLC
FDA (openFDA food enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 12, 2012
OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is indicated for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OmniGuide, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
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 Dec 12, 2012
24 Fr 8mm Sft Flow Str Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Murray's WAFFLE CONE DIP, NET WEIGHT - 7 lb 8 oz (3.40 kg), Product Item Code 835462, Bar code 0 06847 66003 2. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CSM Bakery Products NA
FDA (openFDA food enforcement)
Reported Dec 5, 2012
IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Dec 5, 2012
The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001. The generic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
The Vertex Max Drill Tube is a component within the Navigated Vertex Max Drill Guide Set (item 9733370). The Navigated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
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 Nov 28, 2012
UniCel Dxl 800 Access Immunoassay System, Part Numbers: 973100, A71456, and A71457. The UniCel DxI Immunoassay System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Product is Full OSSEOTITE 2 Tapered Certain Implant, Model Number XIFNT413, and size 4 x 13 mm. The product is sterile.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product 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.