Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,616 in last 12 months

Showing 1044110460 of 13,371 recalls

DrugApril 10, 2015· Medtech Products, Inc.

Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...

The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Hospira Inc.

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

The Issue: Lack of Sterility Assurance: The product has the potential to leak at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 2, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: Acarbose Tablets 50 mg a)10 x 10 Unit Dose Tablets per Blister Pack Recalled...

The Issue: Subpotent Drug: The firm received an out of specification result for Assay...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2015· Cody Laboratories, Inc.

Recalled Item: C-Topical 4% CII (cocaine hydrochloride) Recalled by Cody Laboratories, Inc....

The Issue: Labeling: Label mix-up; bottles were incorrectly labeled as 10 mL instead of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...

The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...

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

Class III — Low RiskOngoing
Refund
DrugMarch 26, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets Recalled by Heritage...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2015· Qualitest Pharmaceuticals

Recalled Item: PROMETHAZINE VC WITH CODEINE SYRUP Recalled by Qualitest Pharmaceuticals Due...

The Issue: Failed Impurities/Degradation Specifications: A stability lot was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

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

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

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

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund