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. 952 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
952 in last 12 months

Showing 48141–48160 of 52,339 recalls

DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Alphahydroxyprogesterone Recalled by Main Street Family Pharmacy, LLC Due to...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: HCG 11000u w/B-12 Recalled by Main Street Family Pharmacy, LLC Due to The...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Minoxidil 10% 60ml Recalled by Main Street Family Pharmacy, LLC Due to The...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Double Strength PGE1 40mcg/ml Recalled by Main Street Family Pharmacy, LLC...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Lipotropic 1.5ml PFS Recalled by Main Street Family Pharmacy, LLC Due to The...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Depo-Testadiiol Recalled by Main Street Family Pharmacy, LLC Due to The firm...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Mic Ultra-Sulfur Free 30ml Recalled by Main Street Family Pharmacy, LLC Due...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Testosterone Cypionate/Propionate 250mg/ml 10ml via Recalled by Main Street...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Lidocaine 1% 30ml (PF) Recalled by Main Street Family Pharmacy, LLC Due to...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Testosterone Cypionate Recalled by Main Street Family Pharmacy, LLC Due to...

The Issue: The firm received seven reports of adverse reactions in the form of skin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2013· DJO, LLC

Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...

The Issue: DJO, LLC has recently identified a product safety issue with the battery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Elekta, Inc.

Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...

The Issue: Customers are resetting the default values outside recommended factory settings.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Beckman Coulter Inc.

Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...

The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...

The Issue: Product labeled with incorrect expiration date.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing