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. 2,452 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,452 in last 12 months

Showing 4344143460 of 52,647 recalls

Medical DeviceSeptember 12, 2014· Eyemart Express Ltd

Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...

The Issue: Prescription eyeglass safety lenses did not meet specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...

The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured

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

Class III — Low RiskOngoing
Medical DeviceSeptember 12, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...

The Issue: The default for normal values are inconsistent between cobas b 221 and other...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2014· Intuitive Surgical, Inc.

Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...

The Issue: Correction due to the detection of a motor sensor failure in the Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...

The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: The Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Ingenuity CT system can mislabel the exposure that results in an image in...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2014· Expo Fresh L.L.C

Recalled Item: Roma Tomatoes Recalled by Expo Fresh L.L.C Due to Potential Salmonella...

The Issue: Expo Fresh is recalling Roma Tomatoes because they have a potential to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 11, 2014· Qualitest Pharmaceuticals

Recalled Item: MethylPREDNISolone TABLETS Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Subpotent; 6 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugSeptember 11, 2014· Hospira Inc.

Recalled Item: HEPARIN SODIUM Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: A particulate, confirmed as human hair, was...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 9, 2014· Hospira Inc.

Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specification: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2014· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...

The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Ortho-Clinical Diagnostics

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

The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Schoitz weights are manual devices used with Schoitz tonometers and Recalled...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Manual bunnell cranial drills are bone cutting and drilling instruments...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Teleflex Medical

Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...

The Issue: The pediatric breathing circuits can crack prior to and during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: McKenzie Perforator Drills are bone cutting and drilling instruments that...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Xoran Technologies, LLC

Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...

The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: An endometrial suction curette is a device used to remove Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: A uterine tenaculum is a hook-like instrument used to seize Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing