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. 1,095 recalls have been distributed to Nebraska in the last 12 months.
Showing 5881–5900 of 49,150 recalls
Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...
The Issue: There is the potential that an electroneurodiagnostic medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGIFOAM" Absorbable Gelatin Powder Kit Recalled by Ethicon, Inc. Due to...
The Issue: Some applicator tips from these lots had open seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into...
The Issue: Quarantined product was inadvertently distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cloderm (clocortolone pivalate) Cream Recalled by EPI Health, LLC Due to...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance Recalled by...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity and Clarity Diagnostics LLC Recalled by Wondfo USA Co Ltd Due to...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well and 2 inch Recalled by Mirion...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System with Well. Intended to be Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) Recalled...
The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System. Intended to be used to Recalled by...
The Issue: Complaints of unexpected detachment of the collimator have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Independent Medical Co-op Inc. Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.