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 Jan 8, 2020
Classic Lays potato chips 2 3/4 oz. UPC 28400 42054; Classic Lays potato chips 8 oz. UPC 28400 19914; Classic Lays…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Frito-Lay, Inc.
FDA (openFDA food enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
STA UNICALIBRATOR (ref. 00675)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fuji Food Products, Inc.
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alliance Tech Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Usage: pre-calibrated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Signal Group Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Siracha HOT Chili Sauce Net Wt. 28 oz. (1 lb. 12 oz.) (793 g); Net Wt. 17 oz. (1 Lb. 1 oz.) in PET Plastic bottles UPC:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Huy Fong Foods, Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2019
Truly Good Foods SOUTH OF THE BORDER nut mix NET CT/WT: 25lb box, CONTAINS: PEANUTS, MILK, AND WHEAT. Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropical Nut & Fruit Company
FDA (openFDA food enforcement)
Reported Dec 18, 2019
Habib EUS RFA, 10mm electrode active tip, Material Number/UPN: 6500 - Product Usage: The Habib EUS RFA is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
CrossCath Support Catheter, RPN CXC3.0-1.9-14-90-P-NS-0, Order Number G51572 For diagnostic and interventional vascular…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Healix Knotless ADV BR 4.75 Suture Anchor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
41 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Quantam 2000 Electrosurgical Generator, Part number 909075.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frog Hollow Farm
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.