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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 3086130880 of 52,647 recalls

FoodMay 30, 2017· ASK Foods Inc

Recalled Item: Taste of Inspirations Recalled by ASK Foods Inc Due to Undeclared Milk

The Issue: A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2017· Hans Kissle Company, LLC

Recalled Item: Whole Foods Cranberry Couscous- packaged in Clear plastic clamshell for 6oz...

The Issue: Product contains undeclared tree nuts-cashews

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 25, 2017· California Sun Dry Foods

Recalled Item: California Sun Dry Sun Dried Tomato Pesto Recalled by California Sun Dry...

The Issue: Firm employee noticed that incorrect back label was attached to Sun-Dried...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Atrium Medical Corporation

Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...

The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: Logic Fit Tibial Tamp Head Recalled by Exactech, Inc. Due to The firm...

The Issue: The firm determined that the labeling (surgical technique) should be updated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Carestream Health Inc

Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...

The Issue: Carestream found a single unit where four screws in the assembly were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...

The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...

The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· NeuroLogica Corporation

Recalled Item: Samsung GU60A system- Digital X-ray Imaging Systems are intended for...

The Issue: When performing the Stitching function on GU60A system, unintended area is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· Northgate Technologies, Inc.

Recalled Item: Electrohydraulic lithotripter probe Recalled by Northgate Technologies, Inc....

The Issue: The inner and outer labels on the product contain incorrect number of...

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

Class II — Potential Health HazardOngoing
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...

The Issue: Presence of foreign substance: The recall was initiated due to black...

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

Class III — Low RiskOngoing
Refund