Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,479 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,479 in last 12 months

Showing 2054120560 of 28,140 recalls

Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64:Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Transport Stretcher Recalled by Stryker Medical Division of Stryker...

The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Abbott Vascular

Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...

The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Perfusion Tubing Pack Recalled by Medtronic Perfusion...

The Issue: Medtronic is notifying customers who have or may receive specific lots of...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 3, 2016· Medical Action Industries Inc

Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...

The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2016· Zimmer Spine, Inc.

Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...

The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of product archiving not working...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...

The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: A migrated study that has annotations will display the annotations, but when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...

The Issue: Communication protocols interfacing with the affected software version with...

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

Class II — Potential Health HazardOngoing