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 2046120480 of 29,284 recalls

Medical DeviceJune 23, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...

The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Olympus Corporation of the Americas

Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...

The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 XPS High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...

The Issue: It was reported that the secondary locking mechanism, and its corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Edan Diagnostics

Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...

The Issue: Incorrect CO2 readings with some patient monitors.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...

The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...

The Issue: Incorrect values for the volume calculation. Software update VB30B via...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Philips Medical Systems Nederlands

Recalled Item: Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product...

The Issue: Certain low-voltage DC power supplies (DCPS) used in these products may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # Recalled by LeMaitre...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products HBsAg Controls Recalled by Ortho-Clinical...

The Issue: The signal/cutoff (s/c) results may increase throughout the...

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

Class III — Low RiskOngoing
Medical DeviceJune 22, 2016· Sorin Group USA, Inc.

Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...

The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anasto AC Closure System and Anasto Universal Clip Remover- Anasto Recalled...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing