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. 1,163 recalls have been distributed to Nebraska in the last 12 months.
Showing 501–520 of 49,150 recalls
Recalled Item: Merck Emend (aprepitant) for oral suspension Recalled by Merck Sharp & Dohme...
The Issue: Presence of particulate matter: potential presence of metal particulates in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...
The Issue: Due to an error when defining a new stereotactic that users fail to first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension...
The Issue: Presence of particulate matter: potential presence of metal particulates in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) CATH LAB Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the Recalled...
The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReBoost Nasal Spray Recalled by Medinatura New Mexico, inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: The products have been...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearLife Allergy Nasal Spray Recalled by Medinatura New Mexico, inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: The products have been...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Recalled...
The Issue: Due to damage to outer tray that can potentially compromise the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conductivity Standard Solution Catalog/Model Numbers: 10001 Recalled by...
The Issue: due to a defect associated with the conductivity values of the solution used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes...
The Issue: Six (6) identified software issues which may result in the following: system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...
The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.