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 981–1000 of 49,150 recalls
Recalled Item: CareLink Clinic Recalled by Medtronic MiniMed, Inc. Due to Software error...
The Issue: Software error causing incorrect data to be displayed on the 24-hour Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow PRUTest Platelet Reactivity Test UDI-DI code: 10711234150078...
The Issue: Due to an device without a premarket clearance being incorrectly package and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SILINTAN 25/pills Recalled by ANTHONY TRINH, 123Herbals LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NIACIN Extended-Release Tablets Recalled by Golden State Medical Supply Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Klarity-C Drops (Cyclosporine) 0.1% Recalled by Imprimis NJOF, LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) Recalled by...
The Issue: Medtronic personnel observed trace amounts of dry blood on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...
The Issue: Potential that product was leak tested with equipment outside of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen 500mg Caffeine 65mg caplets Recalled by Aero Healthcare Due to...
The Issue: Labeling: Label Mix-up. This issue affects the outer box labeling only. The...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...
The Issue: The possibility for this product that is intended for demonstration purposes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...
The Issue: Software application that receives digital images and data to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: If infusion pump is dropped or severely jarred this may damage the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Egg and Cheese Breakfast Burrito Recalled by M.C.I. Foods, Inc. Due to...
The Issue: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.