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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2710127120 of 29,284 recalls

Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Vermed Recalled by Heart Sync, Inc Due to On 4/18/13 HEARTSYNC became aware...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Cardio Medical Products

Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...

The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...

The Issue: Philips has received one report from the field that there was an unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Instratek, Incorporated

Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...

The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2013· Embla System Llc

Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...

The Issue: Calibration error for Embla Embletta Gold units calibrated through service...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· SpineFrontier, Inc.

Recalled Item: Case Lid and Base (Inspan Recalled by SpineFrontier, Inc. Due to Non-toxic...

The Issue: Non-toxic inks, used on the silk screen graphics of the case bases and lids,...

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

Class II — Potential Health HazardOngoing