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. 2,570 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,570 in last 12 months

Showing 1058110600 of 13,381 recalls

DrugJanuary 25, 2015· Detox Transforms

Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 23, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 23, 2015· Mylan Institutional LLC

Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2015· Sun Pharma Global Fze

Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: 6 month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2015· Sun Pharma Global Fze

Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...

The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2015· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...

The Issue: Non-Sterility: Product tested positive for bacterial contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 20, 2015· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; Hospira has identified the particulate as a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 20, 2015· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...

The Issue: Non-Sterility: Product tested positive for bacterial contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2015· Noven Pharmaceuticals, Inc.

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

The Issue: Defective Delivery System: One lot exceeded the mechanical peel specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 8, 2015· Freedom Pharmaceuticals Inc

Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugJanuary 6, 2015· American Health Packaging

Recalled Item: Benzonatate Capsules Recalled by American Health Packaging Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: Virazole (Ribavirin for Inhalation Solution Recalled by Valeant...

The Issue: Non-Sterility: Valeant's laboratory observed a positive microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2014· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Loratadine Syrup (Loratadine Oral Solution) 5 mg/5 mL Recalled by...

The Issue: Presence of Foreign Substance: Presence of blue plastic floating in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2014· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: The firm received a complaint of an embedded...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2014· Baxter Healthcare Corp.

Recalled Item: Fluconazole Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints of leaks due to an incomplete...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2014· Qualitest Pharmaceuticals

Recalled Item: ACETAMINOPHEN and CODEINE PHOSPHATE ORAL SOLUTION USP Recalled by Qualitest...

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

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

Class III — Low RiskOngoing
Refund
DrugDecember 22, 2014· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product has the potential for solution...

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

Class II — Potential Health HazardOngoing
Refund