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. 2,816 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,816 in last 12 months

Showing 98419860 of 29,496 recalls

Medical DeviceMay 7, 2021· K2M, Inc

Recalled Item: Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2...

The Issue: Mislabeled product labeling incorrect length or height, or length and height...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2021· Corin Ltd

Recalled Item: Corin TriIFit TS SIZE 2 Recalled by Corin Ltd Due to Units from one batch of...

The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2021· Corin Ltd

Recalled Item: Corin TriFit CF SIZE 7 Recalled by Corin Ltd Due to Units from one batch of...

The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2021· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear....

The Issue: Potential that a limited number of individual contact lens packages have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400A Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400T Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: WorkMate Claris v.1.2 Upgrade Kits Recalled by Abbott Laboratories Inc. (St...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens...

The Issue: Photometer Lamp May Reach Saturation Without Flagging Results, may generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: Recalled...

The Issue: Ortho investigated and confirmed the potential for unexpected failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing