All recall categories

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.

Medical devices

Reported Aug 21, 2024

HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thoratec LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hoff & Pepper, Co. LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2024

Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medivance Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Prophet Premium Blends, LLC

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2024

Abbott Infinity 5, Implantable Pulse Generator, REF: 6660, SterileEO, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

TourniKwik Tourniquet Set (CFN 79012)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX analyzers are intended for: " In Vitro testing of samples…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Impella CP with SmartAssist, Product No.: 1000080 (REF 0048-0003). left heart support blood pump

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Canadian Hospital Specialties Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C. Krueger Finest Baked Goods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Echonous Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2024

GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Vingmed Ultrasound As

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

Hudson Harvest Tomato Basil Sauce, 16 oz., UPC # 683720301567

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hudson Harvest Wholesale

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.