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 2728127300 of 52,647 recalls

Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· NxStage Medical, Inc.

Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...

The Issue: There is a potential risk of electrical fire when fluid leaks into the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Withings Sas

Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...

The Issue: Device could not meet the requirements for systolic pressure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
FoodJune 11, 2018· Absonutrix

Recalled Item: Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Recalled by...

The Issue: The firm was informed that the product did not contain vitamin B12...

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

Class III — Low RiskOngoing
Refund
FoodJune 8, 2018· T R Toppers, Inc.

Recalled Item: TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075...

The Issue: Recalling TR Toppers Brand Chopped Chocolate Pretzel Pieces due to the...

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

Class II — Potential Health HazardOngoing
Refund