Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,696 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,696 in last 12 months

Showing 1962119640 of 29,496 recalls

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· 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· 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 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· 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 15, 2016· BioMerieux SA

Recalled Item: ETEST Imipenem IP32 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 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¿ Ceftriaxone TXL32 SPB 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 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 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 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 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: 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 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
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Fosfomycin FM1024 Blister 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 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 12 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 16 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 10 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing