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. 2,730 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,730 in last 12 months

Showing 51615180 of 52,647 recalls

Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT HP2 DB SLIT 3.0MM ANGCE Recalled by...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK SATINCRESCENT FULL HANDLE2.3MM ANG...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY SLIT SB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: ClearCut S Safety Sideport Knife 1.2mm Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
FoodJuly 15, 2024· Pariva LLC

Recalled Item: Pariva Marinated Labneh Bites Za'atar Recalled by Pariva LLC Due to Product...

The Issue: Product may be contaminated with mold.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 15, 2024· Pariva LLC

Recalled Item: Pariva Marinated Labneh Bites Mild Tandoori Recalled by Pariva LLC Due to...

The Issue: Product may be contaminated with mold.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 15, 2024· Pariva LLC

Recalled Item: Pariva Marinated Labneh Bites Rosemary Garlic Recalled by Pariva LLC Due to...

The Issue: Product may be contaminated with mold.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 15, 2024· Omnia Medical

Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...

The Issue: Failure of fusion system instruments in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Omnia Medical

Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...

The Issue: Failure of fusion system instruments in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2024· SoloVital

Recalled Item: Umary Acido Hialuronico Recalled by SoloVital Due to Undeclared Diclofenac

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2024· Supercore Products Group Inc.

Recalled Item: Gold Hard Steel Plus Liquid Recalled by Supercore Products Group Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2024· Supercore Products Group Inc.

Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing