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 2660126620 of 29,284 recalls

Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts >or= 6mm Intended for use in arterial Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SuperSoft Grafts >or= 6mm Intended for use in arterial Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene IFG with Assisted Delivery Intended for use in arterial Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular Recalled...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Bifurcated Grafts >or= 6mm Intended for use in Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts >or= 6mm Intended for use in arterial vascular...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel AIR 84 Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: Complaints were received from the field indicating that some Air Pumps were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2013· Cayenne Medical Inc.

Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...

The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....

The Issue: Software issue results in inaccurate 3D image may result in ablation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing