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 3242132440 of 52,647 recalls

Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 20x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental vss bowed 19x190mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 16x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 14mmdx48cm right Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Tibial IM Nail 15mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: HYFRECATOR 2000 HANDPIECE SHEATH Recalled by ConMed Corporation Due to For...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Stryker Communications

Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...

The Issue: The potential hazard that can arise for the combination of the missing...

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2017· Versa Marketing

Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...

The Issue: Product was tested and found positive for Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2017· Whole Food Market

Recalled Item: Whole Foods Market King Cake Recalled by Whole Food Market Due to Undeclared...

The Issue: Product contains undeclared pecans

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

Class I — Serious Health HazardOngoing
Refund