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 Mar 12, 2025

Paradigm REF: MMT-712 and MMT-715

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

Medtronic MiniMed, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14,…

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

Micro Therapeutics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Philips IntelliSpace Cardiovascular software, Model 830089.

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

Philips Medical Systems Nederland B.V.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2025

DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.

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

Beckman Coulter Laboratory Systems (suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2025

BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis…

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

CareFusion 303, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2025

Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER…

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

Nestle-USA, Inc. (Corporate Office)

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 26, 2025

Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STATEMENT: Processed in a gluten-free and…

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

Apna Wholesale Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2025

DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2025

AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Soft Plum Aloo Bukahara 1/2 LB; *May…

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

Global Commodities Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2025

3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US…

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

Kci USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2025

LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2025

THREE RIVERS brand TUTTI-FRUTTI; INGREDIENTS Papaya Cubes, Sugar, Citric Acid (E-330), Potassium Sorbate (E-202), FD&C…

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

Shata Traders Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2025

Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In…

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

HF Acquisition Co. LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

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

Max Mobility LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2025

NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark Chocolate / Vegan. 12g Protein

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

Bazzini LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 12, 2025

COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES

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

D. Coluccio & Sons Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2025

Temporary Titanium Abutments

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

DDS Lab

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…

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

Ethicon, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN:…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve…

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

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based…

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

Medicrea International

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2025

Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side…

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

Mutual Trading Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2025

NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL…

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

Neilmed Pharmaceuticals Inc.

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.