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 2822128240 of 52,647 recalls

Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: TWO PART ADAPTER Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: CATHETER REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F MODIFIED Tesio CATHETER SET Recalled by Medical Components, Inc dba...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga (S/M) Recalled by Stryker Instruments Div. of Stryker...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Zipper Toga with Peel-Away Face Shield Recalled by Stryker Instruments...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Sofradim Production

Recalled Item: Versatex Monofilament Mesh 50 x 50cm Recalled by Sofradim Production Due to...

The Issue: There have been patient reports of abdominal hernia recurrence following...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Zipper Toga with Peel-Away Face Shield Recalled by Stryker Instruments...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Get The Tea

Recalled Item: Life Change Fat Burner Recalled by Get The Tea Due to Get The Tea is...

The Issue: Get The Tea is notifying customers that Life Change Fat Burners contain soy.

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

Class II — Potential Health HazardOngoing
Refund