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. 1,025 recalls have been distributed to Nebraska in the last 12 months.
Showing 18641–18660 of 49,150 recalls
Recalled Item: Knee Products: 183742 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 184762 Knees Vanguard Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Weight-Low Volume Blood Transport System for...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Set Prime Line - Product Usage: is Recalled by Baxter...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: TMJPM-1510 Microfixation Custom Made Device Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Spin Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: The unplugging of the main cable on the monitor trolley from the X10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 189260 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Transport System for Hemodialysis Blood Set -...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
The Issue: Incorrect IOL diopter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...
The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...
The Issue: This product has been confirmed to exhibit holes in the packaging, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...
The Issue: There is potential for a white paper-type residue attached to the catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: low out of specification (OOS) test result observed in long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KORE ORGANIC CBD Oil Watermelon 15mg* Recalled by Summitt Labs Due to...
The Issue: Chemical Contamination; product contains elevated levels of lead
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nizatidine Oral Solution Recalled by Amneal Pharmaceuticals of New York, LLC...
The Issue: CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Plus 1.25 mg Capsule Recalled by MasterPharm LLC Due to Cross...
The Issue: Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Recalled by B & B Pharmaceuticals, Inc. Due to Foreign Object...
The Issue: cGMP deviations: Presence of foreign material (Teflon)introduced at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.