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 48,100 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.
Reported Apr 27, 2022
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
New England Beach Pizza 1. Extra Cheese 2. Cheese
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beach Brand Foods LLC
FDA (openFDA food enforcement)
Reported Apr 27, 2022
ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DNA Genotek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Matrix Clinical Solution At-Home COVID-19 Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Matrix Medical Network
FDA (openFDA device enforcement)
Reported Apr 27, 2022
therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deerfield Imaging, Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Graphic Controls Acquisition Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Integra Universal Flexible Arm part number REF 1362275
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
LIPOSORBER System, Model: LA-15, consisting of: Apheresis machine, product# 101445 model: MA-03, and disposables…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kaneka America Corp.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Cub 2 Enclosed Bed Canopy System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sensory Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skippy Foods, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2022
IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Volcano Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Alinity m HBV Application Specification File (US and CE)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Bread Alone Fruit & Nut Sourdough; packaged in 27 ounce plastic bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bread Alone, Inc.
FDA (openFDA food enforcement)
Reported Apr 13, 2022
Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brius Technologies Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
1. Wegmans 10oz Watermelon Chunks 2. Wegmans 32oz Watermelon Chunks 3.Fresh Harvest 18oz Watermelon Chunks 4. Tops…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fruit Fresh Up, Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2022
Panther Fusion GBS Assay Cartridges 96 Tests, Catalog Number: PRD-04484. in vitro diagnostic test for group b…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
MODEL: X-RAY R/F SYSTEM FLUOROspeed X1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
BenchMark ULTRA and DISCOVERY ULTRA Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corporation
FDA (openFDA device enforcement)
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Other states
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.