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. 2,574 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,574 in last 12 months

Showing 2136121380 of 52,647 recalls

Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund