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 25, 2016
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamedix Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumenis Ltd.
FDA (openFDA device enforcement)
Reported May 25, 2016
Organic Green Tea Hojicha, Net 16 kgs, (bulk product 16 kg boxes with inner liner)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qtrade Teas And Herb
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 25, 2016
Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 25, 2016
COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unfi
FDA (openFDA food enforcement)
Reported May 18, 2016
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
FDA (openFDA device enforcement)
Reported May 18, 2016
Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom Unite Connect for Nurse Call (version 2.2.0).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascom US, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bradshaw Medical Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
Poly-bags containing splint strap labeled with "Pediatric" sticker. Each strap kit contains adjustable length leg…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
NORVEN herring in oil, Net Wt. 17.6 oz. (500g), UPC barcode 856687004196, and Net Wt. 10.6 oz. (300g), UPC barcode…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olma-Xxi Inc.
FDA (openFDA food enforcement)
Reported May 4, 2016
Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported May 4, 2016
Bliss French Vanilla Ice Cream 64oz Product Code: 51051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bliss Bros Dairy, Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System 12mm X 30mm Material Number: M00576550 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 4, 2016
Trinity Acetabular System Product Usage - Total Hip Replacement.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin USA Limited
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2016
Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2016
Family Gourmet Long Grain Enriched White Rice, 32 oz. (2 lb.) plastic bag (SKU: 1218898)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Family Dollar Stores - NC Distribution Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
Dunkin Donuts Brand Italian Sub, Net Wt 7.7 oz packaged in Bag, Clear View
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flying Food Group LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
Hardy Diagnostics GBS Detect Cat no. A300. Used for the isolation and detection by enhanced hemolysis of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported May 4, 2016
CF InPlex ASR Card; Catalog Number: 95-0501.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 4, 2016
Drew Scientific Inc. Drew3-PAC. This D3 Reagent Pack includes: diluent reagent 5L, enzymatic cleaner 750 mL, and a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jas Diagnostics/Drew Scientific
FDA (openFDA device enforcement)
Reported May 4, 2016
RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
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.