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. 1,733 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,733 in last 12 months

Showing 4536145380 of 49,150 recalls

Medical DeviceMay 15, 2013· Maytex Corp

Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...

The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Day/Night Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Warming Relief Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Nighttime Warming Relief Nighttime Multi-Symptom Cold Recalled by...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Actavis South Atlantic LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL Recalled by Actavis...

The Issue: Failed Impurity/Degradation Specification; "Related Compound C"

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Nighttime Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Excedrin Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Budesonide Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Dissolution Specifications: Routine stability testing at the 12-month...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
FoodMay 15, 2013· Arthur Schuman Midwest LLC

Recalled Item: GRATED 2/25 GRANA PADANO Recalled by Arthur Schuman Midwest LLC Due to...

The Issue: Grated Grana Padano Hard Italian Cheese was tested and found to be positive...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Optovue, Inc.

Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...

The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...

The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...

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

Class II — Potential Health HazardOngoing