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. 1,752 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,752 in last 12 months

Showing 4586145880 of 52,647 recalls

Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2013· Tendex

Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Vitality Research Labs LLC

Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Fougera Pharmaceuticals Inc.

Recalled Item: KETOCONAZOLE CREAM Recalled by Fougera Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification degradant...

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

Class III — Low RiskOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 5/15 sulfite-free (5% Amino Acid in 15% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: 50 mg Nitroglycerin in 5% Dextrose Injection (200 mcg/mL) Recalled by Baxter...

The Issue: Presence of Particulate Matter; particulate matter in one vial identified as...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 4.25/25 sulfite-free (4.25% Amino Acid in 25% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Fossil Fuel Products, LLC

Recalled Item: RezzRX capsules Recalled by Fossil Fuel Products, LLC Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: Fossil Fuel Products, is recalling...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 18, 2013· Brainlab AG

Recalled Item: Brainlab Recalled by Brainlab AG Due to The "fluoro match registration"...

The Issue: The "fluoro match registration" function of the Navigation Software Spine &...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 4-7 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Lite Blood Glucose Test Strips Recalled by Abbott Diabetes Care,...

The Issue: Certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Strata II Shunt Assembly Kit Recalled by Medtronic Neurosurgery...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: CSF-Unitized Shunt Recalled by Medtronic Neurosurgery Due to Medtronic...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 2-3 Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 2-3 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing