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 48,122 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.

Medical devices

Reported Nov 28, 2012

IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and…

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

Innovative Magnetic Resonance Imaging Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Inspan…

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

SpineFrontier, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature

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

Vital Signs Colorado Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator…

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

Vital Signs Devices, a GE Healthcare Company

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2012

Peanut Butter Pave, UPC code 693868102117 & 69386905312, in the following sizes: 1) 5 Piece Peanut Butter Pave, 63…

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

B.T. McElrath Chocolatier, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2012

PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…

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

Dako North America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2012

Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…

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

Progressive Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2012

Whole Foods Meal Shrimp Stir Fry, 16 oz plastic container, Refrigerated, Product Code 3640630222

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

Whole Foods Market Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2012

Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…

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

Clinical Diagnostic Solutions

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2012

Starbucks Protein Bistro Box, Net Wt 6.8 OZ (193g), Contains Cage-free egg, white Cheddar Cheese, multigrain muesli…

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

Flying Food Group, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 14, 2012

Hannaford Red Velvet Cake Truffle, 6 count UPC #20335800000

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

Hannaford Bros.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 14, 2012

Earthbound Farms Organic Baby Spinach Grab & Go Salad; with sesame, soy vinaigrette and peanuts. USDA Organic 3.5 oz.…

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

Natural Selection Foods LLC dba Earthbound Farm

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2012

Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2012

"***Sharpoint IQ Geometry Slit Knife Angled, Bevel Up***Surgical Specialties Corporation Reading, PA***REF 72-2740***"…

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

Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2012

HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…

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

Heartsine Technologies, Limited

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2012

Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…

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

Progressive Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

Osseotite Tapered Certain Implant 5 X 10mm Model INT510 Biomet 3i Dental Implants are intended for surgical placement…

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

Biomet 3i, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage…

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 31, 2012

Natural Honey Peanut Butter; 16 oz jars, UPC 855188003035; Natural Honey Peanut Butter Squeeze Packs 0.5 oz, UPC…

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

Justin's Nut Butter

7 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 31, 2012

Label reads in part "*** ORGANIC Alden's ICE CREAM PEANUT BUTTER 'n CHIP 1.5 QTS ***" upc 0 72609 74191 2.

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

Oregon Ice Cream, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 31, 2012

Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…

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

Terumo Cardiovascular Systems Corporation

5 more products in this recall

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.