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. 2,725 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,725 in last 12 months

Showing 1234112360 of 29,154 recalls

Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Acutus Medical AcQGuide Mini Fixed-Curve Introducer with AcQCros QX...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Rhythm Xience Guider Catheter Introducer with Lancer Intergrated...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· Butterfly Network, Inc.

Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...

The Issue: Distributed without an approved 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· Butterfly Network, Inc.

Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...

The Issue: Distributed without an approved 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· LivaNova USA Inc.

Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...

The Issue: The firm is providing validated cleaning and disinfection instructions in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Qiagen Sciences LLC

Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...

The Issue: An image on the associated polybag contains an incorrect rinse time of 30...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Philips North America, LLC

Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...

The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Radiometer Medical ApS

Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...

The Issue: Reports have been received about the transcutaneous monitoring system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Avalon Elite Vascular Access Kit Recalled by Maquet Cardiovascular Us Sales,...

The Issue: A lot of Avalon Elite Vascular Access Kits (VAK) are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2020· Haemonetics Corporation

Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...

The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing