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. 1,910 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,910 in last 12 months

Showing 2632126340 of 52,339 recalls

Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar Powerpack-Visub(V3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS SUITE Recalled by Philips Electronics North America Corporation Due...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si/X/Xi Surgical System Redundant Medical Grade Power Supply...

The Issue: Certain Redundant Medical Grade Power Supply (RMGPS) units specific to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIura Xper F010 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlIura Xper F010 F Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010/10 DRTable Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: NTEGRIS Allura 9 0 FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (mono) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution...

The Issue: Immersion time stated on the bottle is 45 minutes while the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...

The Issue: Analyzers were distributed with software which lacks a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...

The Issue: The product was mislabeled with the incorrect label.

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

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

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

Class II — Potential Health HazardOngoing