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. 2,755 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,755 in last 12 months

Showing 97019720 of 13,449 recalls

DrugAugust 19, 2015· Pharmakon Pharmaceuticals

Recalled Item: Ketamine 50 mg/mL Recalled by Pharmakon Pharmaceuticals Due to Stability...

The Issue: Stability data does not support expiry.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2015· Pharmakon Pharmaceuticals

Recalled Item: Provocholine Pre-diluted Set II in 0.9% Sodium Chloride Recalled by...

The Issue: Stability data does not support expiry.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2015· Pharmakon Pharmaceuticals

Recalled Item: Midazolam (PF) 0.5 mg/mL in 0.9% Sodium Chloride Recalled by Pharmakon...

The Issue: Subpotent drug.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2015· Apotex Inc.

Recalled Item: Cevimeline Hydrochloride Capsules Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Stability Specifications: product may not meet specification limit...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2015· Bausch & Lomb, Inc.

Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Cream (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban (mupirocin calcium) Nasal Ointment Recalled by GlaxoSmithKline,...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Mupirocin Calcium Cream Recalled by GlaxoSmithKline, LLC. Due to Penicillin...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2015· Blue Square Market, Inc.

Recalled Item: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG) Recalled by Blue...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 6, 2015· Blue Square Market, Inc.

Recalled Item: KABOOM action strips Recalled by Blue Square Market, Inc. Due to Undeclared...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 6, 2015· 3M Company - Health Care Business

Recalled Item: DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and...

The Issue: Chemical contamination: Product may be contaminated with a toxic compound.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2015· Taro Pharmaceuticals, Inc.

Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...

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

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

Class III — Low RiskOngoing
Refund