Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,771 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,771 in last 12 months

Showing 58015820 of 13,449 recalls

DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine HCL Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/ Recalled by...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due to...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Recalled by Sun...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP 10 mcg Recalled by Glenmark Pharmaceuticals...

The Issue: Defective Delivery System: Estradiol Vaginal Inserts USP plunger is not...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Double Strength Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Iron Supplement Elixir Ferrous Sulfate Recalled by Geritrex, LLC...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: Zileuton Extended-Release Tablets Recalled by Chiesi USA, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Diphenhydramine Oral Liquid Alcohol Free Recalled by Geritrex, LLC Due to...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Children & Adults Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Diocto Liquid Docusate Sodium Stool Softener Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium) Recalled by...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: ZYFLO CR (zileuton) extended-release tablets Recalled by Chiesi USA, Inc....

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund