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. 2,644 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,644 in last 12 months

Showing 1600116020 of 52,647 recalls

Medical DeviceJuly 26, 2021· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...

The Issue: Due to potential performance issues with software version 3.2.3 and earlier....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick Recalled by...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad Large Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Swabstick (3's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad MEDIUM Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodide Cleansing Scrub Swabstick (3's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidine Iodine Swabstick (1's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2021· Mivi Neuroscience Inc

Recalled Item: MIVI Super 90 8F Guide Catheter Recalled by Mivi Neuroscience Inc Due to...

The Issue: There is potential for nonsterility of product due to a possible defect in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Mivi Neuroscience Inc

Recalled Item: MIVI Super 90 Guide Catheters Recalled by Mivi Neuroscience Inc Due to There...

The Issue: There is potential for nonsterility of product due to a possible defect in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Aspen Surgical Products, Inc.

Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...

The Issue: Affected products were manufactured with materials found to have a bioburden...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Aspen Surgical Products, Inc.

Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....

The Issue: Affected products were manufactured with materials found to have a bioburden...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Aspen Surgical Products, Inc.

Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....

The Issue: Affected products were manufactured with materials found to have a bioburden...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· BioMimetic Therapeutics, LLC

Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...

The Issue: The kit contains the wrong vial tray in the package.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Boston Scientific Corporation

Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...

The Issue: Potential for leaks and loosening at the patient catheter connection

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2021· Boston Scientific Corporation

Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...

The Issue: Potential for leaks and loosening at the patient catheter connection

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

Class II — Potential Health HazardOngoing