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. 2,436 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,436 in last 12 months

Showing 3138131400 of 49,150 recalls

FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 14, 2016· Akorn Inc

Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications; out-of specification value for homogeneity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2016· Ultimate Body Tox

Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 12, 2016· KRAFT HEINZ FOODS COMPANY

Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...

The Issue: Possible contamination of product with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...

The Issue: A review of packaging revealed the seal integrity of the pouch may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...

The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Halyard Health, Inc

Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...

The Issue: Drapes within the affected lots may include a manufacturing variation that...

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

Class II — Potential Health HazardOngoing
FoodNovember 9, 2016· Seth Ellis Chocolatier, LLC

Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...

The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...

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

Class I — Serious Health HazardOngoing
Refund