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. 2,437 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,437 in last 12 months

Showing 4988149900 of 52,647 recalls

FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks Recalled by...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights ALMOND Natural Flavor Coconut Haystacks Recalled by Island...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2013· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...

The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...

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

Class I — Serious Health HazardOngoing
DrugJanuary 7, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Belladonna Alkaloids (hyoscyamine sulfate Recalled by West-ward...

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots were found in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2013· Somersault Snack Co., LLC

Recalled Item: Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds...

The Issue: During ingredient review for kosher certification, the firm discovered that...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2013· Reumofan Plus USA

Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active

The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 4, 2013· Actavis Pharmaceuticals

Recalled Item: buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed Dissolution Specifications; 8-hours for the 18-month stability...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
DrugJanuary 3, 2013· Mobius Therapeutics LLC

Recalled Item: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...

The Issue: Non-Sterility: one or more components of the kit have been found to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2013· Animas Corporation

Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...

The Issue: Animas has identified a component issue affecting a small supply of the...

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

Class I — Serious Health HazardOngoing
FoodJanuary 2, 2013· EonNutra, LLC

Recalled Item: Growth Factor Complex 200 GFC 200 Recalled by EonNutra, LLC Due to Eon...

The Issue: Eon Nutra, LLC is recalling certain SOTO Supplements GFC 200 because the...

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

Class II — Potential Health HazardOngoing
Refund