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. 2,491 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,491 in last 12 months

Showing 1844118460 of 49,150 recalls

Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK SET SCREW Recalled by...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 11 HOLE 197MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 7 HOLE 140MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: Biomet 6.5 Cannulated Screw Tap - Bone fixation screw Recalled by Biomet Due...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. T15 Multi-Directional Locking Screw 3.5mm x 60mm Recalled by Biomet...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
DrugMay 14, 2020· InvaGen Pharmaceuticals, Inc.

Recalled Item: Gabapentin Tablets USP Recalled by InvaGen Pharmaceuticals, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; failure of Impurity A test at...

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2020· West-Ward Columbus Inc

Recalled Item: Doxycycline Hyclate Tablets USP Recalled by West-Ward Columbus Inc Due to...

The Issue: Failed dissolution specification: The dissolution test at the 24 month time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2020· West-Ward Columbus Inc

Recalled Item: Ethacrynic Acid Tablets USP Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Med Tec Inc

Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...

The Issue: Potential for disengagement of the Varian Style Type-S Extension during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing