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. 2,715 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,715 in last 12 months

Showing 68416860 of 29,284 recalls

Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Preat Corp

Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...

The Issue: Engaging titanium base contains a dimensional condition that allows vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: There are technical issues related to signal generation and processing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...

The Issue: There are technical issues related to signal generation and processing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· Moberg Research, Inc.

Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...

The Issue: Battery leakage can cause corrosion to the metal enclosure near the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2023· AGILENT TECHNOLOGIES INC./US

Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...

The Issue: Distributed sample collection kit with an unapproved instruction for use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 17, 2023· RAYSEARCH LABORATORIES AB

Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...

The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing