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. 1,930 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,930 in last 12 months

Showing 2082120840 of 29,154 recalls

Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...

The Issue: The versions allow images to be stored without pixel data, resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Bit Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Fastener...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Plate Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity...

The Issue: Philips Healthcare received reports from the field that certain Ingenuity...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Appliance...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The...

The Issue: Philips Healthcare received reports from the field that certain Ingenuity...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. cannula...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Orthopedic...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Applied Medical Resources Corp

Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...

The Issue: Increased customer complaints indicating inconsistent clip application; may...

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

Class II — Potential Health HazardOngoing