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. 1,926 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,926 in last 12 months

Showing 2244122460 of 29,154 recalls

Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Leica Microsystems, Inc.

Recalled Item: The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments....

The Issue: The ASP6025 Tissue Processor instrument is incorrectly getting into a state...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Cepheid

Recalled Item: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50...

The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...

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

Class III — Low RiskOngoing
Medical DeviceJuly 27, 2015· Cepheid

Recalled Item: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number...

The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...

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

Class III — Low RiskOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Zippie IRIS Wheelchair. model EIZ5A in combination with option code Recalled...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Advanced Sterilization Products

Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing