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. 1,765 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,765 in last 12 months

Showing 4362143640 of 52,339 recalls

Medical DeviceMay 28, 2014· Childrens Medical Ventures

Recalled Item: Gel-E Donut Recalled by Childrens Medical Ventures Due to The gel-filled...

The Issue: The gel-filled Gel-E Donut and Squishon product line has received a number...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerators of type ARTISTE Recalled by Siemens Medical...

The Issue: A safety risk exists with automatically sequenced treatment technique using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

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

Class I — Serious Health HazardOngoing
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled by Navitas,...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 27, 2014· Dot Foods Inc.

Recalled Item: Large Pitted Kalamata Olives Recalled by Dot Foods Inc. Due to This...

The Issue: This voluntary recall has been initiated because Savor Brands Large Pitted...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2014· BioFire Diagnostics, Inc.

Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...

The Issue: BioFire has identified an increased risk of false positive results when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2014· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Cardiovascular Systems, Inc.

Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...

The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing