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. 2,527 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,527 in last 12 months

Showing 3278132800 of 52,647 recalls

Medical DeviceFebruary 2, 2017· Elcam Medical, Inc.

Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...

The Issue: The stopcock was found to have punctures.

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2017· Sandoz Inc

Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...

The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Sage Products Inc

Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System...

The Issue: It was found that during a procedure the Peak Skin Dose (PSD) value...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Nidek Inc

Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...

The Issue: During treatment planning, the procedure was programmed with an unintended...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...

The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Beckman Coulter Inc.

Recalled Item: iChemVELOCITY Urine Chemistry System Recalled by Beckman Coulter Inc. Due to...

The Issue: The probe misalignment or bending has the potential to lead to delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Hidrex GmbH

Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...

The Issue: The device was reclassified from a class III device to a class II device and...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 30, 2017· Tearscience, Inc

Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...

The Issue: Labeling: The labeled storage temperature is not consistent with the...

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

Class II — Potential Health HazardOngoing