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. 2,400 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,400 in last 12 months

Showing 3760137620 of 49,150 recalls

Medical DeviceMay 21, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...

The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...

The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· CooperSurgical, Inc.

Recalled Item: MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 Recalled by CooperSurgical,...

The Issue: A diaphragm size 80 labeled box was incorrectly packaged with a size 85.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...

The Issue: Bacterial contamination.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 20, 2015· Mylan Lab Inc

Recalled Item: Mycophenolic Acid Delayed-release Tablets Recalled by Mylan Lab Inc Due to...

The Issue: Failed Dissolution Specifications: Low out of specification dissolution results.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2015· Hospira Inc.

Recalled Item: Magnesium Sulfate Injection Recalled by Hospira Inc. Due to Failed pH...

The Issue: Failed pH Specifications: 12 month stability testing

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 19, 2015· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...

The Issue: A reduction in the reconstituted stability has been identified. Clinicians...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2015· Edwards Lifesciences, LLC

Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...

The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2015· Zimmer, Inc.

Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...

The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: GLUTATHIONE 200MG/ML (STERILE WATER) (30ML Recalled by Advanced Physician...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: SODIUM HYALURONATE (STERILE WATER) 2.5 ML VIAL 20MG/ML INJECTABLE Recalled...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: ESTRADIOL CYPIONATE (SESAME OIL) (10ML Recalled by Advanced Physician...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: VITAMIN D3 (OLIVE OIL) (30ML VIAL) 50 Recalled by Advanced Physician...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: SODIUM TETRADECYL (STERILE WATER) 30ML VIAL 2% INJECTABLE Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: CYANOCOBALAMIN (PARABEN WATER) (10ML Recalled by Advanced Physician...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund