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. 2,753 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,753 in last 12 months

Showing 1632116340 of 29,496 recalls

Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution EVO 3.6 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Digital Ready Recalled by GE Healthcare, LLC Due to DIGITAL...

The Issue: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 520 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT 160 1.5D STD WAUK Recalled by GE Healthcare, LLC Due to Some...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: CT Goldseal BrightSpeed 16 PWR TIO 2 YR Recalled by GE Healthcare, LLC Due...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Fort Defiance Industries, LLC

Recalled Item: FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER Recalled...

The Issue: During long-term storage (i.e. military depot), the interaction of stagnant...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Two...

The Issue: Two lots of tibial bearings were commingled. There is a possibility that a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Anesthesia Machine Recalled by Draeger Medical, Inc. Due...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Perseus A500 Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: This email is to provide notification that, due to a software bug that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...

The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing