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. 1,132 recalls have been distributed to Nebraska in the last 12 months.
Showing 1921–1940 of 49,150 recalls
Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: YoCrunch Lowfat Yogurt with Toppers Recalled by DANONE US LLC Due to Foreign...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BritePro Solo Mini with Pro Miller Blade Size 1.5 Recalled by Flexicare...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BritePro Solo Single-Use Fiber Optic Laryngoscope Handle :040-310AU and...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shave and Skincare Power Stick Original Nourishing Invisible Protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beauty & Skincare Power Stick original nourishing invisible protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bicillin L-A (penicllin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.