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.
Showing 20101–20120 of 28,140 recalls
Recalled Item: ACUSON SC2000 Ultrasound imaging system with software version VB10C and...
The Issue: While imaging with a transesophageal (TEE) transducer (Z6Ms, V5Ms, or V7M),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...
The Issue: The potential exists within the identified tables that incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Confocal GI Scope Product Usage: Intended to provide optical visualization...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...
The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. Product Usage: Merge Hemo is a hemodynamic Recalled by...
The Issue: In some instances, the system will lock tabs within a study, even when a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...
The Issue: Use of the software may show an incorrect value to the user when viewing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSpore 4 mL Ampoule Biological indicator for steam sterilization Recalled...
The Issue: Product resistance has fallen outside of label claim within expiry.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...
The Issue: An error message can occur resulting in the prior studies being unavailable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: When taking measurements from images on the Cardio workstation or from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...
The Issue: The software produced a number of "do not route" exceptions, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...
The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.