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. 2,820 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,820 in last 12 months

Showing 77017720 of 13,536 recalls

DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pfizer Inc.

Recalled Item: Sterile Water for Injection Recalled by Pfizer Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 500 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2017· Pfizer Inc.

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Pfizer Inc. Due to...

The Issue: Presence of Particulate Matter: glass particulate found in vial

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2017· Lucky Mart Inc.

Recalled Item: PIYANPING Anti-Itch (hydrocortisone) Lotion Recalled by Lucky Mart Inc. Due...

The Issue: Incorrect Product Formulation: product contains dexamethasone instead of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2017· Amerisource Health Services

Recalled Item: Enalapril Maleate Tablets Recalled by Amerisource Health Services Due to...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Mild Healthcare Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Choice Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP Deviations;...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

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

Class II — Potential Health HazardOngoing
Refund