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. 2,527 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,527 in last 12 months

Showing 3316133180 of 52,647 recalls

DrugDecember 16, 2016· Aurobindo Pharma USA Inc

Recalled Item: Pantoprazole Sodium for Injection Recalled by Aurobindo Pharma USA Inc Due...

The Issue: Discoloration: Some vials were found to contain powder with a...

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2016· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2016· TIPIAK Inc

Recalled Item: Tipiak Pearled Couscous Easy cooking 12.3 Oz (350g) Item Number: Recalled by...

The Issue: Product may contain foreign metal fragments

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2016· Parker Medical

Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...

The Issue: The product was not functioning as intended. The ventilation to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM Recalled...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension AMM (DF119)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) 9cm prosthesis Recalled by Zimmer Biomet,...

The Issue: labeling for specific lots of the Standard OSS Modular Proximal Tibia...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Covidien LLC

Recalled Item: Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10 Recalled by Covidien...

The Issue: Labeling error: The label indicates the product is latex free, but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy...

The Issue: An error can occur causing Delta corrections to be lost when one setup field...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· DICOM GRID INC

Recalled Item: Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version...

The Issue: A software error caused the window/level to become the same in one series...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT with software version 4.7.0 Product Usage: The Recalled by...

The Issue: Multiple issues have caused the device to result in CT rescans or incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Doripenem DOR32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftriaxone TXL32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Vancomycin VA 256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftazidime TZ256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Gentamicin GM256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: Ciprofloxacin CI 32 Foam packaging Recalled by BioMerieux SA Due to Product...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Cephalotin CE 256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Benzyl Penicillin PG256 FOAM packaging Recalled by BioMerieux SA Due...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Tobramycin TM256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing