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. 2,765 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,765 in last 12 months

Showing 761780 of 52,647 recalls

Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Accriva Diagnostics, Inc.

Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...

The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Cepheid

Recalled Item: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10. Recalled by Cepheid Due to...

The Issue: Product testing did not meet expected stability criteria.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2025· Datascope Corp.

Recalled Item: Cardiosave Rescue. Intra-Aortic Balloon Pump system. Recalled by Datascope...

The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2025· Datascope Corp.

Recalled Item: Cardiosave Hybrid. Intra-Aortic Balloon Pump system. Recalled by Datascope...

The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GVS TM, Inc

Recalled Item: SQ40S Blood Transfusion Filter Recalled by GVS TM, Inc Due to Due to...

The Issue: Due to products being released for distribution prior to completion of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Recalled...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX"...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Recalled...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Organic Acids Profile Test Large Recalled by GET TESTED INTERNATIONAL AB Due...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing