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. 2,732 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,732 in last 12 months

Showing 1134111360 of 29,154 recalls

Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Boston Scientific Corporation

Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...

The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is...

The Issue: Potential sterility issue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· C-RAD POSITIONING AB

Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...

The Issue: PC Application Software c4D not changing Site upon synchronization during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Talladium Inc

Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...

The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...

The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing