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. 2,466 recalls have been distributed to Nebraska in the last 12 months.
Showing 21981–22000 of 49,150 recalls
Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...
The Issue: There is a risk to the healthcare professional or patient of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811961 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229034A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811910...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top (Model #1161640) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229003A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Pyrophosphate Kit Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentreotide (10 uGm) Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...
The Issue: Multiple complaints were received for balloons bursting below the rated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm Recalled by Teleflex Medical Due to...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan: 1) CF 6.0 mm Recalled by Teleflex Medical Due to This...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.