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. 2,632 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,632 in last 12 months

Showing 3404134060 of 53,621 recalls

Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Legacy Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Innova 2000 Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestilix Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCV+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige SI Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCA Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Precision 500D Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige VH Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Tepha Incorporated

Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...

The Issue: Endotoxin values from testing of retains slightly exceeded the established...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Oculus Innovative Sciences, Inc.

Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...

The Issue: Firm became aware that professional samples of Ceramax are not meeting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2016· Shimadzu Medical Systems

Recalled Item: Shimadzu X-ray High Voltage Generator Model No. UD150B-40 on SONIALVISION...

The Issue: Shimadzu Medical Systems is recalling the Shimadzu X-ray High Voltage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Teleflex Medical

Recalled Item: WECK Visistat 35W Recalled by Teleflex Medical Due to Sterility Deficiency:...

The Issue: Sterility Deficiency: The packages are not sealed properly and thus the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: IWS Infant Warmer System-Infant radiant warmers provide infrared heat...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Omnibed- The OmniBed is a combination...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator Ohmeda Medical Giraffe Incubator-The Giraffe Incubator is...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing