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. 1,901 recalls have been distributed to Nebraska in the last 12 months.
Showing 19461–19480 of 49,150 recalls
Recalled Item: Allura Exper FD Series. System codes 722003 722010 722022 722005 Recalled by...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly G Integris H5000 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clover seed in 55 lb. multi-layered white paper bags Recalled by...
The Issue: Possible contamination with E. Coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clover seed in 50 lb. woven poly bags Recalled by International Sprout...
The Issue: Possible contamination with E. Coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresh From Meijer diced hard boiled eggs sold by weight Recalled by Meijer...
The Issue: Possible L. mono contamination in hard boiled eggs
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dawson-Mueller Drainage Catheter Recalled by Cook Inc. Due to Specific lots...
The Issue: Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP...
The Issue: Failed Tablet/Capsule Specifications: Complaints related to crumbling of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: Chemical contamination; out of specification results obtained for equipment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: US Clinical 20mL Programmable Pump. Catalog No. 01827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 91827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable 20mL Pump. Catalog No. 93827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 40mL Pump. Catalog No. 16827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 11827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...
The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.