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. 1,858 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,858 in last 12 months

Showing 3404134060 of 53,621 recalls

Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: RFX 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: 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: 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: 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: 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: ADVANTX LCLP+ 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 LCN+ 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: SFX 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: Prestige II 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· 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
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Lidocaine HCl 1% Recalled by Cantrell Drug Company Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Oxytocin 30 USP Units Added to 0.9% Sodium Chloride Recalled by Cantrell...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Calcium Chloride Recalled by Cantrell Drug Company Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 2 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Heparin Sodium Recalled by Cantrell Drug Company Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 1 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Ropivacaine HCl 0.25% in 0.9% Sodium Chloride Recalled by Cantrell Drug...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund