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. 2,479 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,479 in last 12 months

Showing 2076120780 of 49,150 recalls

Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2019· American Health Packaging

Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 26, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...

The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2019· Natures One Inc

Recalled Item: PediaSmart Organic Soy Vanilla Beverage Mix Recalled by Natures One Inc Due...

The Issue: Undeclared milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 26, 2019· Hometown Food Company

Recalled Item: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix Recalled by...

The Issue: Product tested positive for gluten but is labeled as Gluten free

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2019· Tuscano and Delucia Group (DBA Entropic Labs)

Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...

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

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2019· Philips North America, LLC

Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...

The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Ra Medical Systems, Inc.

Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...

The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: fexofenadine hydrochloride tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine HCL Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochrloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine HCl) tablets USP Recalled by Aurolife Pharma,...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (fexofenadine hydrochrloride) tablets Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2019· Thoratec Switzerland GMBH

Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...

The Issue: Reports have been received of the CentriMag Systems experiencing motor and...

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

Class I — Serious Health HazardOngoing