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 1966119680 of 29,284 recalls

Medical DeviceOctober 31, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...

The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Owens & Minor Distribution, Inc.

Recalled Item: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA Recalled by Owens...

The Issue: Owens & Minor is the initial importer and private label distributor of Medi...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Hologic, Inc

Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....

The Issue: Breach in sterile barrier compromising product sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Natus Medical Incorporated

Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...

The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· The Binding Site Group, Ltd.

Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...

The Issue: A change in the calibration curve causing an increase in false prozone flags.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Aesculap Implant Systems LLC

Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...

The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Ion Beam Applications S.A.

Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...

The Issue: IBA is initiating this recall to address an issue identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA...

The Issue: Possible unintentional x-ray emission after users attempt early termination...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· 3M Company - Health Care Business

Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...

The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...

The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 25, 2016· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...

The Issue: Disengaged screw head could potentially not be retained in the Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...

The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...

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

Class II — Potential Health HazardOngoing