Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,747 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,747 in last 12 months

Showing 3592135940 of 48,330 recalls

DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: TopCare LORATIDINE 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: Sunmark 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: Safeway Care 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: CVS Pharmacy Recalled by Ohm Laboratories, Inc. Due to Superpotent Drug: Out...

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: Rite Aid Pharmacy loratadine orally disintegrating tablets USP 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: 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: 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: 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: 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 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· 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: 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: 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: 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: Equaline 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: 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: Health Mart 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
Medical DeviceJuly 28, 2015· Beckman Coulter Inc.

Recalled Item: Access Thyroglobulin Assay Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter, Inc. is recalling Access Thyroglobulin reagent packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics...

The Issue: When both ports (Serial and Ethernet) are configured to transmit data, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing