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. 2,511 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,511 in last 12 months

Showing 3648136500 of 52,647 recalls

Medical DeviceMarch 28, 2016· Stryker Endoscopy

Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...

The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Philips Ultrasound, Inc.

Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...

The Issue: The fasteners securing the control panel assembly to the base of the Philips...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2016· B. Braun Medical Inc

Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Non-Sterility: fungal contamination due to leaking containers.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 25, 2016· Bryant Ranch Prepack Inc.

Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...

The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Monteris Medical Corp

Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...

The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2016· Hansen Medical Inc

Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...

The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...

The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2016· Lupin Limited

Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· AbbVie Inc.

Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 24, 2016· Teleflex Medical

Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...

The Issue: Incorrect expiration date was printed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing