Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,495 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,495 in last 12 months

Showing 2038120400 of 28,579 recalls

Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...

The Issue: System locks up which may result in potential patient injury or delay in...

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: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...

The Issue: Cardio study list does not show STAT studies without .

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: 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 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· 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· 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. Pin 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· Biomet, Inc.

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

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· 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· 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· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. guide 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· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Screw 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· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...

The Issue: Reports of failure of the device's power supply.

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· Biomet, Inc.

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

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. Arthroscope....

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. 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· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...

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

Class II — Potential Health HazardOngoing