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. 2,547 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,547 in last 12 months

Showing 2424124260 of 52,647 recalls

FoodMarch 28, 2019· Iowa Corn Processors

Recalled Item: Yellow Corn Flour #620 Recalled by Iowa Corn Processors Due to Foreign...

The Issue: Product could contain foreign objects (pliable blue plastic)

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2019· Boston Salads & Provisions Co., Inc.

Recalled Item: Edamame Salad sold under the following labels: BOSTON SALADS Prepared...

The Issue: Possible metal fragment contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
FoodMarch 27, 2019· Theo Chocolate Inc

Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...

The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2019· Medi-Physics Inc. dba GE Healthcare

Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...

The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 26, 2019· Molnlycke Health Care, Inc

Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...

The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2019· Lohxa LLC

Recalled Item: Bismuth Subsalicylate Oral Suspension 262mg/15mL Recalled by Lohxa LLC Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2019· Lohxa LLC

Recalled Item: Phenobarbital Oral Solution Recalled by Lohxa LLC Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Lightning Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing