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. 1,938 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,938 in last 12 months

Showing 2004120060 of 29,154 recalls

Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Natus Medical Incorporated

Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...

The Issue: The firm sent the Technical Bulletin to consignees who received the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· GE Healthcare, LLC

Recalled Item: Brivo XR385 Recalled by GE Healthcare, LLC Due to The placing of weight on...

The Issue: The placing of weight on the VRAD detector, of the Brivo XR385 digital...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Keystone Dental Inc

Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...

The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: Image data for a patients image may not be correct

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...

The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2016· Hand Biomechanics Lab Inc

Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...

The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· TEM Systems Inc

Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...

The Issue: Customers complained of low/empty reagent vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Contour Fabricators Inc

Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...

The Issue: Two customer complaints suggest that excessive rotation of the cable in one...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Celerity ECG Cable Accessory Pack Recalled by Angiodynamics Inc. (Navilyst...

The Issue: The Celerity ECG Cable Accessory Pack has the potential to contain an ECG...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...

The Issue: Ortho confirmed that it is possible for the mis-association of sample...

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

Class II — Potential Health HazardOngoing