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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2908129100 of 52,647 recalls

FoodOctober 30, 2017· 21ST CENTURY SNACK FOODS

Recalled Item: 21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered...

The Issue: Product contains undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2017· ICU Medical Inc

Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...

The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2017· ICU Medical Inc

Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...

The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2017· NordicNeuroLab AS

Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...

The Issue: Report was of an interrupted MR scan after patient complained about acoustic...

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 27, 2017· L3 Security & Detection

Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...

The Issue: L3 has determined in airport environments, there have been several cases...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Large Cheese Filled Cannoli Recalled by Wegmans Food Markets, Inc....

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Marshmellow Treats Tub Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Single Cheese Cannoli Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Cheese Cannoli Tray Recalled by Wegmans Food Markets, Inc. Due to Undeclared Soy

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Marshmellow Treat sold by the pound Recalled by Wegmans Food...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Dark Bulk Penny Choc Coins Recalled by Wegmans Food Markets, Inc....

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Mini Cheese Filled Cannolis 4pk Recalled by Wegmans Food Markets,...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing