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. 1,008 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,008 in last 12 months

Showing 37601–37620 of 52,647 recalls

Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK213 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Teva North America

Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...

The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2015· Northeast Laboratory Services, Inc.

Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...

The Issue: Product marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...

The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Baxter Corporation Englewood

Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...

The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing