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. 2,543 recalls have been distributed to Nebraska in the last 12 months.
Showing 16161–16180 of 28,140 recalls
Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ MULTI 2 SDIL Recalled by Siemens Healthcare Diagnostics,...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Travel Kit Recalled by Madison Polymeric Engineering Due to The products...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad with 4" Button Brush Recalled by Madison...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draco Enzymatic Deep-Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...
The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...
The Issue: There is a potential for the connection screw of the stem extractor to break.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.