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 Dec 30, 2020

MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…

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

Cook Inc.

20 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2020

CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ (396g) Canyon Bakehouse, LLC Johnstown, CO 80534 UPC 8…

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

Flowers Foods (Corporate Offices)

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

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

ICU Medical, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2020

CACAO MARKET MARIE BELLE NEW YORK; Dark Chocolate Pearls; Ingredients: Cocoa bean, sugar, biscuit cereals (wheat flour,…

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

Maribel's Sweets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 30, 2020

Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

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

Nova Ortho-Med Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 23, 2020

Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4…

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

Dreyers Grand Ice Cream, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 23, 2020

Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF…

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

Galt Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product…

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

Kowa Optimed Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…

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 Dec 16, 2020

MAC VU360, Electrocardiograph

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

Golden Boy brand Custard muffin Original; 7.76 ounce, rigid clear plastic packages

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

Hong Thai Foods Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 16, 2020

On the Go Sweet & Salty Trail Mix

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

Kanan Enterprises Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

PROKERA, non-sterile - Product Usage: Biologic corneal bandage.

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

TissueTech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.

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

Veg Pro International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

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

Welch Allyn, Inc/mortara

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or…

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

CME America, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da…

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

Advanced Bionics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

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.