Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,756 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,756 in last 12 months

Showing 4418144200 of 52,647 recalls

Medical DeviceMay 29, 2014· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an oncology information system used to manage Recalled by...

The Issue: MOSAIQ does not re-calculate the agent volume when the user changes the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Kerr Corporation

Recalled Item: Tytin Regular Set Recalled by Kerr Corporation Due to Kerr Corporation is...

The Issue: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Elekta, Inc.

Recalled Item: iGUIDE System Product Usage: The intended use of the device Recalled by...

The Issue: A bug in the software prevents the iGUIDE software from logging off.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Synthes, Inc.

Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....

The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 29, 2014· Teva Pharmaceuticals USA

Recalled Item: Fluvastatin Capsules USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2014· Novartis Pharmaceuticals Corp.

Recalled Item: Foradil Aerolizer (formoterol fumarate inhalation powder) Recalled by...

The Issue: Failed Stability Specification; out of specification result for particle...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled by Navitas,...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Childrens Medical Ventures

Recalled Item: Gel-E Donut Recalled by Childrens Medical Ventures Due to The gel-filled...

The Issue: The gel-filled Gel-E Donut and Squishon product line has received a number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing