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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 1041–1060 of 49,150 recalls
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine Hydrochloride Recalled by STAQ Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % Recalled by USV...
The Issue: Failed Impurities/Degradation Specifications: The result for 'Any individual...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sucralfate Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCL PF Recalled by STAQ Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL Citrate PF Recalled by STAQ Pharma, Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...
The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...
The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.