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. 2,406 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,406 in last 12 months

Showing 4398144000 of 52,339 recalls

DrugMay 16, 2014· US Compounding Inc

Recalled Item: ePHEDrine Sulfate Injection Recalled by US Compounding Inc Due to Mislabeling

The Issue: Labeling: Label Error on Declared Strength; The outer light protective bags,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug.

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Biomet, Inc.

Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...

The Issue: Surface finish is different than specified. The implant has 30 grit blast on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Ebi, Llc

Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...

The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...

The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...

The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Synthes, Inc.

Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...

The Issue: All lots of B37 Replacement Screws are being recalled due to potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Chemistry Controls Level I and II LEVl: Amber Recalled by...

The Issue: The original mean assigned to the control too high, upon reassignment with...

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

Class III — Low RiskOngoing
FoodMay 15, 2014· Hot Mama's Foods

Recalled Item: Spicy Yellow Lentil Hummus sold under the Eat Well Embrace Recalled by Hot...

The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2014· Hot Mama's Foods

Recalled Item: 5 Layer Fiesta Dip sold under the Trader Joe's brand Recalled by Hot Mama's...

The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2014· Hot Mama's Foods

Recalled Item: Chipotle Hummus sold under the Giant Eagle Market District brand Recalled by...

The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2014· Hot Mama's Foods

Recalled Item: Garlic Hummus sold under the Giant Eagle Market District brand Recalled by...

The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund