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 2596125980 of 29,284 recalls

Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use...

The Issue: Stryker has identified a potential for the auger and/or cannula to fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 30MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand SUPER COMPLIANT 7MM X 15MM Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 150CM 2 TIP Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Medline Industries Inc

Recalled Item: Mucus Specimen Trap 40 cc Recalled by Medline Industries Inc Due to There is...

The Issue: There is a potential that the specified mucus specimen traps are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand GDC-18 360 18MM X 30CM Recalled by Stryker Neurovascular Due...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 10MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Acetabular Pressurizer Recalled by Stryker Instruments Div. of Stryker...

The Issue: On March 14, 2013 a Work Order was opened for 120 units (20 boxes) of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral...

The Issue: Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen...

The Issue: Two complaints were received in which it was reported that the stem would...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions...

The Issue: Hospira has received customer reports of broken door assemblies on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 30, 2013· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular...

The Issue: Maquet has received an increase in the number of complaints for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand-N-Weigh Recalled by Ergosafe Products LLC DBA...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand Recalled by Ergosafe Products LLC DBA Prism...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Philips Medical Systems, Inc.

Recalled Item: Easy Diagnost Eleva Universal Fluoroscopic applications Recalled by Philips...

The Issue: The delivered application software was an outdated version to the model of...

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

Class II — Potential Health HazardOngoing