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. 2,834 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,834 in last 12 months

Showing 57815800 of 53,621 recalls

Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Integra LifeSciences Corp.

Recalled Item: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical...

The Issue: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential for certain Life2000 ventilator systems to either fail to charge...

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

Class I — Serious Health HazardOngoing
FoodMay 28, 2024· U.B.C. Food Distributors INC.

Recalled Item: Baraka brand ground black pepper packaged in 7oz retail containers Recalled...

The Issue: Potential Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Consumer Product Partners, LLC

Recalled Item: Petroleum Jelly Recalled by Consumer Product Partners, LLC Due to Labeling:...

The Issue: Labeling: Label Mix up; product labeled as pure white petroleum jelly...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2024· Winder Laboratories, LLC

Recalled Item: Phenazopyridine HCl Tablets USP Recalled by Winder Laboratories, LLC Due to...

The Issue: Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2024· Sagent Pharmaceuticals

Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...

The Issue: Presence of Particulate Matter: Presence of particulate matter from the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

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

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Sagent Pharmaceuticals

Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...

The Issue: Presence of Particulate Matter: Presence of particulate matter from the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

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

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing