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. 2,574 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,574 in last 12 months

Showing 1910119120 of 29,284 recalls

Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set with Injection Site and 0.2 micron filter Recalled by...

The Issue: CareFusion is recalling the MaxGuard Extension Set with Injection Site and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Medtronic Sofamor Danek USA Inc

Recalled Item: Poly Component Trial Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The dovetails of poly trials, Beta 2.0, were observed as either cracked or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Medtronic Sofamor Danek USA Inc

Recalled Item: Poly Component Trial Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The dovetails of poly trials, Beta 2.0, were observed as either cracked or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Merit Medical Systems, Inc.

Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 15, 2017· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit. Dialyzer Recalled by Baxter Healthcare Corporation...

The Issue: Firm has received reports of device operators failing to adhere to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2017· IntroMedic Co., Ltd.

Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...

The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2017· Zimmer Biomet, Inc.

Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...

The Issue: Digital templates were created with the incorrect files.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2017· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Chemistry Analyzer AU680/AU5800 Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the Rack ID Labels because the Rack ID number...

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

Class II — Potential Health HazardOngoing