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. 2,622 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,622 in last 12 months

Showing 86618680 of 13,371 recalls

DrugSeptember 2, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Hyoscyamine Sulfate Recalled by VIRTUS PHARMACEUTICALS OPCO II L Due to...

The Issue: Failed Content Uniformity Specifications: resulting in both superpotent and...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2016· Actavis Laboratories, FL, Inc.

Recalled Item: Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 29, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Sandoz Inc

Recalled Item: Phenylephrine HCI Injection Recalled by Sandoz Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Sandoz Inc

Recalled Item: Ephedrine Sulfate Injection Recalled by Sandoz Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2016· Impax Laboratories, Inc.

Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...

The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 19, 2016· Unichem Pharmaceuticals Usa Inc

Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...

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

Class III — Low RiskOngoing
Refund