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. 1,062 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,062 in last 12 months

Showing 22381–22400 of 53,621 recalls

DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: SUCCinylcholine Chloride (PF) Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Norepinephrine added to 5% Dextrose (PF) Recalled by KRS Global...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· Pfizer Inc.

Recalled Item: Zarontin (ethosuximide capsules Recalled by Pfizer Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2019· Pfizer Inc.

Recalled Item: ethosuximide capsules Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco M2734A Recalled by Pacific Medical Group Inc. Due to Fetal/maternal...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Tocotransducer (Nautilus) Recalled by Pacific Medical Group...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco+ transducer with ECG/IUP capability (wired) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M2736A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V680 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-UI Assy Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing