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. 2,678 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,678 in last 12 months

Showing 1326113280 of 29,284 recalls

Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2019· Tomtec Imaging Systems Gmbh

Recalled Item: TOMTEC-ARENA TTA2 Recalled by Tomtec Imaging Systems Gmbh Due to The firm...

The Issue: The firm discovered a software issue associated with the Image-Com...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Potential for calibration error resulting in QC failures after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Ra Medical Systems, Inc.

Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...

The Issue: The firm has become aware there is a potential problem with its DABRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· CrossRoads Extremity Systems, LLC

Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...

The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing