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. 997 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
997 in last 12 months

Showing 40061–40080 of 53,621 recalls

DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Leader Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets Recalled by...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Premier Value Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Fresenius Kabi USA, LLC

Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...

The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Novartis Pharmaceuticals Corp.

Recalled Item: Dexmethylphenidate HCl Extended-Release Recalled by Novartis Pharmaceuticals...

The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Wal-itin Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Up&Up loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Health Best Choice Care Recalled by Ohm Laboratories, Inc. Due to...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Fred's Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: CareOne Original Prescription Strength Recalled by Ohm Laboratories, Inc....

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Major loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: HEB Loratadine Orally Disintegrating Tablets Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: QC Quality Choice Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Discount Drug Mart Food Fair Recalled by Ohm Laboratories, Inc. Due to...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Ohm Loratadine Orally Disintegrating Tablets Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Meijer Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 27, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for z-statistic related to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing