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. 2,787 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,787 in last 12 months

Showing 1168111700 of 13,536 recalls

DrugMarch 14, 2014· Shire Human Genetic Therapies, Inc.

Recalled Item: VPRIV¿ (velaglucerase alfa for injection) Recalled by Shire Human Genetic...

The Issue: Presence of Particulate Matter; Particulates identified as stainless steel...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 13, 2014· Blu Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Tablets USP 500 mg Recalled by Blu Pharmaceuticals...

The Issue: Defective container: Product distributed without inner seal on bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2014· Blu Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Tablets USP 1000 mg Recalled by Blu Pharmaceuticals...

The Issue: Defective container: Product distributed without inner seal on bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...

The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may containin a syringe...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Effexor XR (venlafaxine HCl) Extended-Release Capsules Recalled by Pfizer Us...

The Issue: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 6, 2014· Greenstone Llc

Recalled Item: Venlafaxine HCl Extended-Release Capsules Recalled by Greenstone Llc Due to...

The Issue: Presence of Foreign Tablets/Capsules: report of a foreign capsule with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Alkermes, Inc.

Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) Recalled by...

The Issue: Customer complaints for failure to deliver the dose.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...

The Issue: Lack of Assurance of Sterility; leaking of premix bags

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo-Fort DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex PORTABLE SIPS 5X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not DROPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund