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. 2,710 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,710 in last 12 months

Showing 82018220 of 29,284 recalls

Medical DeviceMay 19, 2022· C.R. Bard Inc

Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...

The Issue: Complaints relating to urine output measurement accuracy.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· DePuy Orthopaedics, Inc.

Recalled Item: MODULAR CATHCART FRACTURE HEAD HIP BALL Recalled by DePuy Orthopaedics, Inc....

The Issue: The Cathcart Ball has an inherent +5mm offset which is not currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...

The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...

The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Radiometer Medical ApS

Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...

The Issue: There is a potential for sporadic incidents of positive and negative biases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2022· Baxter Healthcare Corporation

Recalled Item: #1 MAC F/O LARYNGOSCOPE Recalled by Baxter Healthcare Corporation Due to...

The Issue: Packaging error.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2022· Draeger Medical, Inc.

Recalled Item: Drager SafeStar 55 Recalled by Draeger Medical, Inc. Due to Possible...

The Issue: Possible occlusion of filters due to manufacturing error.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2022· Rayner Intraocular Lenses Ltd

Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...

The Issue: The outer package is mislabeled and the package contains a different IOL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2022· Covidien, LP

Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...

The Issue: The affected staplers have the potential for the staple guide to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
Medical DeviceMay 11, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2022· GE Healthcare, LLC

Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...

The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing