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 91619180 of 13,371 recalls

DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 80 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 20 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 40 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Bonita Pharmaceuticals, LLC

Recalled Item: Menthocin Patch with Lidocaine-Strong (Menthol 5% Recalled by Bonita...

The Issue: Marketed without an approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 10 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Amerisource Health Services

Recalled Item: Candesartan Cilexetil Tablets Recalled by Amerisource Health Services Due to...

The Issue: Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

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

The Issue: Presence of Particulate Matter: identified as cardboard.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...

The Issue: Presence of Particulate Matter: identified as dried skin.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: identified as a cloth fiber.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

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

The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Amerisource Health Services

Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...

The Issue: Failed Dissolution Specifications: Unexplained low out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2016· Master Herbs, Inc./Li

Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...

The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.

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

Class I — Serious Health HazardOngoing
Refund