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. 1,161 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,161 in last 12 months

Showing 1501–1520 of 52,647 recalls

Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2025· Berkeley Advanced Biomaterials, LLC

Recalled Item: Tribio Implant 7.5mm x 40mm SB008 UDI code: Recalled by Berkeley Advanced...

The Issue: Due to incorrect product label (Incorrect product name identified on outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2025· LeMaitre Vascular, Inc.

Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...

The Issue: The bovine carotid arteries used to produce the impacted grafts from...

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

Class II — Potential Health HazardOngoing
DrugSeptember 2, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...

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
DrugSeptember 2, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...

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
DrugSeptember 2, 2025· AvKARE

Recalled Item: Norgestimate and Ethinyl Estradiol Tablets Recalled by AvKARE Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Non_DEHP Extenstion Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CONTINU-FLO Solution Set Recalled by Baxter Healthcare Corporation Due to IV...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Getinge Disinfection Ab

Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...

The Issue: Potential for device to overheat during operation if the circulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model...

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing