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. 1,777 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,777 in last 12 months

Showing 4664146660 of 53,621 recalls

DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Super Fat Burning Bomb Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: JIANFEIJINDAN Activity Girl Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· Teva Pharmaceuticals USA

Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 100 mg were manufactured...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Pill for weight reduction Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizitang Strong Version Botanical Slimming Recalled by MyNicNaxs, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Fruta BIO 400 mg capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Slim Xtreme Weight loss capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: REDUCE WEIGHT FRUTA PLANTA Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Magic Slim capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Clarity Medical Systems Inc

Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...

The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...

The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hologic, Inc

Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...

The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2014· Smith & Nephew Inc

Recalled Item: Interfit Shell Recalled by Smith & Nephew Inc Due to Inner spherical radius...

The Issue: Inner spherical radius of the shell is undersized.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2014· Atricure Inc

Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...

The Issue: The firm was notified by a customer of a cracked spring in the handle of the...

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

Class II — Potential Health HazardOngoing