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. 2,752 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,752 in last 12 months

Showing 16211640 of 52,647 recalls

DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Lactated Ringers's Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 18, 2025· CORNEAT VISION, LTD.

Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed...

The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· CORNEAT VISION, LTD.

Recalled Item: EverPatch+ Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have...

The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· Boston Scientific Corporation

Recalled Item: ICEfx Cryoablation System Recalled by Boston Scientific Corporation Due to...

The Issue: Certain desiccant tube subassemblies were built with end caps that were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· Boston Scientific Corporation

Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...

The Issue: Certain desiccant tube subassemblies were built with end caps that were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...

The Issue: Potential for activation of an abnormal alarm pause.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· ETHICON, LLC

Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...

The Issue: Potential for barb non-engagement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing