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 2856128580 of 29,284 recalls

Medical DeviceJune 15, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...

The Issue: The recall was initiated because Carefusion has identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Diagnostica Stago, Inc.

Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...

The Issue: Following a single customer complaint that incorrect INR values were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Ge Healthcare It

Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...

The Issue: Multiple issues were identified with the GE Centricity PACS-IW system that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Philips Healthcare Inc.

Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...

The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Integra Life Sci.

Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...

The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Teleflex Medical

Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...

The Issue: Speaker Failure. If the speaker fails and an event occurs which would...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Carestream Health, Inc.

Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...

The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware through complaints of a potential safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2012· Tedan Surgical Innovations Llc

Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...

The Issue: This letter is to notify you that several of our sterile screw products are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Gold Rover (120 Vand 230V ) Waste Management Recalled by Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Neptune Bronze Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing