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. 2,606 recalls have been distributed to Nebraska in the last 12 months.
Showing 10541–10560 of 49,150 recalls
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...
The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow...
The Issue: No label on packaged product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein- In vitro diagnostic use Recalled by Randox...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SmartPath to Ingenia Elition X MR System Recalled by Philips North...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR 7700 System Recalled by Philips North America Llc Due to Gradient...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ingenia Elition S MR System Recalled by Philips North America Llc...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ingenia Elition X MR System Recalled by Philips North America Llc...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Upgrade to MR 7700 System Recalled by Philips North America Llc Due...
The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allergy Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Fetal Spiral Electrode-intended for patients requiring fetal heart...
The Issue: Fetal Spiral Electrode (FSE) spiral tip of the FSE breaking off during use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Chocolate II Agar- IVD for the isolation and cultivation Recalled by...
The Issue: Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica MICROSYSTEMS M530 OHX Recalled by Leica Microsystems, Inc. Due to...
The Issue: There is a potential issue resulting in the Power Supply potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica MICROSYSTEMS Provido Recalled by Leica Microsystems, Inc. Due to There...
The Issue: There is a potential issue resulting in the Power Supply potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica MICROSYSTEMS Proveo 8 Recalled by Leica Microsystems, Inc. Due to...
The Issue: There is a potential issue resulting in the Power Supply potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.