Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,576 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,576 in last 12 months

Showing 85218540 of 13,381 recalls

DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Indiomin MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2016· Akorn Inc

Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...

The Issue: Subpotent Drug: concentration of product is less than labeled amount.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

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

Class III — Low RiskOngoing
Refund
DrugOctober 19, 2016· Janssen Ortho L.L.C.

Recalled Item: Invokamet (canagliflozin and metformin HCl) tablets Recalled by Janssen...

The Issue: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2016· GSK Consumer Healthcare

Recalled Item: Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to...

The Issue: Labeling Not Elsewhere Classified: front labels have the incorrect NDC or...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2016· Town and Country Compounding and Consultation Services, LLC

Recalled Item: HCG (Chorionic Gonadotropin Lyopholized) II Recalled by Town and Country...

The Issue: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: due to out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2016· Pharmedium Services, LLC

Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2016· Par Pharmaceutical, Inc.

Recalled Item: Travoprost Ophthalmic Solution USP Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Lack of Assurance of Sterility; damage to the internal portion of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceutical

Recalled Item: PredniSONE Tablets USP Recalled by West-Ward Pharmaceutical Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Phenobarbital Tablets Recalled by West-Ward Pharmaceuticals Corp. Due to...

The Issue: Failed Dissolution Specifications: Phenobarbital Tablets have an out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2016· Amerisource Health Services

Recalled Item: Paricalcitol Capsules Recalled by Amerisource Health Services Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: This repackaged product was...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit Hardcase - Product Code 85-0889 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund