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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 7141–7160 of 28,140 recalls
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: 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.
Recalled Item: The 4Kscore Test is an in vitro serum or plasma Recalled by BioReference...
The Issue: SPM software anomalies that may lead to the generation of erroneous 4Kscore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Packs IV START TRAY I-Intended for IV Recalled by...
The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Packs IV START KIT-Intended for IV Access Recalled...
The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Packs IV START KIT- Intended for IV Recalled by...
The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III Recalled by...
The Issue: Internal comparison studies revealed unacceptable, light staining. Light...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline CISION Sterile Blades. Labeled as follows with corresponding Item...
The Issue: Potential of the blade puncturing the outer foil layer causing a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeVilbiss Recalled by DeVilbiss Healthcare LLC Due to The firm has received...
The Issue: The firm has received complaints of the device becoming hot. The firm has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Natus Cranial Access Kit is designed to be a complete Recalled by Natus...
The Issue: Due to Cranial Access Kits containing recalled sterile surgical drapes. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Controlled Electrosurgical Suction Coagulator Recalled by ConMed...
The Issue: Suction ports may potentially be occluded on the affected devices. If this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.