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.
4,307 stored notices name Massachusetts, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
Reported Jul 17, 2024
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zoll Medical Corporation
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jul 10, 2024
BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2024
First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.First Source Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jul 10, 2024
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens AG/Siemens Healthcare GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter ULT16.0-38-25-P-6S-MCL-HC--Intended for percutaneous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Global Mix Inc.
FDA (openFDA food enforcement)
Reported Jul 3, 2024
COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
22 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2024
The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mermaid Medical A/S
FDA (openFDA device enforcement)
Reported Jul 3, 2024
NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NovaSignal Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
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.