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. 2,624 recalls have been distributed to Nebraska in the last 12 months.
Showing 5901–5920 of 49,150 recalls
Recalled Item: Captus 4000e Thyroid Uptake System. Intended to be used to Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well. Intended to be Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well and 2 inch Recalled by Mirion...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) Recalled...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance Recalled by...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution Recalled by Revive Rx LLC dba...
The Issue: Labeling: Label Mix-up - product labeled as tirzepatide contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amphotericin B Liposome for Injection Recalled by SUN PHARMACEUTICAL...
The Issue: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...
The Issue: Event Catalog information does not save when copied and transferred from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...
The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...
The Issue: The required leakage test was not performed following of a re-work for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...
The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.