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.

4,307 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.

Medical devices

Reported Dec 25, 2024

Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An…

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

CooperSurgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual…

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

Fabalish,

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

Galaxy System (GAL-001)

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

Noah Medical

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the…

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

Spacelabs Healthcare, Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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)

Medical devices

Reported Dec 18, 2024

Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x…

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

Hermes Medical Solutions AB

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

Nestle Health Services Nutren 2.0 kCal/mL, Calorically Dense Complete Nutrition with Fiber Unflavored. 1000mL (1.1QT).…

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

Nestle Health Science

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2024

Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy…

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

Noah Medical

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

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

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2024

(1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC 21291600000) (2) GREEN CHICKEN ENCHILADAS 6 CT SS COLD (UPC…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)

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

Cartiva, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.

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

Philips North America LLC

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2024

Wegmans Large Asian Sesame Salad with Chicken and Asian Peanut Dressing.

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

Wegmans Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

AMS Artificial Urinary Sphincter Control Pump

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)

Food

Reported Dec 4, 2024

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

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

Curio Spice Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

TriALTIS TORQUE LIMITER, RATCHET, 11.3 Nm, Model Number 5161-00-5048 (G919509)

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

Gauthier Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR…

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

R. Walters Foods, Limited Liability Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL

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

Shimadzu Corp. Analytical & Measuring Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor…

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

Enchroma 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.