The Recall Desk

State

Nebraska product recalls

73,833 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,580
Critical
713
Severe
1,345
Most recent
2026-10-28

Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59476–59500 of 78413

  • HighFDA (Devices)·Z-0857-2015·2014-12-31

    Iris Diagnostics Recalls RTH8 Rotor for StatSpin Express 4 Centrifuge

    Iris Diagnostics is recalling RTH8 rotors for the StatSpin Express 4 Horizontal Centrifuge because the parts may develop cracks with use over time.

    Product
    RTH8 Rotor, P/N X01-005847-001. RTH8 used in the StatSpin Express 4 Horizontal Centrifuge, Model M510, Product No. SSH4. The RTH8 rotor is used with the Statspin Express 4 Horizontal Centrifuge. StatSpin Express 4 Centrifuge: For in vitro diagnostic use to produce the rapid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0856-2015·2014-12-31

    Horiba Lite DM Software Recall for Potential Data Mismatch

    Horiba Instruments is recalling Lite DM software versions 2.0.0.19 and lower due to a bug that may apply test results to the wrong patient order.

    Product
    Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and lower Product Model #: D00A00224D The Lite DM (Lite Data Manager) is a software application developed by HORIBA Medical intended to receive, store, and manage Startup, Patient, and Quality Control (QC)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0874-2015·2014-12-31

    Ebi Solitaire-C Cervical Spacer Drill Sleeves Recalled for Design Deficiency

    Ebi, LLC is recalling 193 units of Solitaire-C Cervical Spacer System drill sleeves because a design defect allows instruments to penetrate 1.0 mm beyond intended depths.

    Product
    Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Drill/Awl Sleeve Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0326-2015·2014-12-31

    Neolpharma Recalls Subpotent Alprazolam Tablets Nationwide

    Neolpharma, Inc. is voluntarily recalling 12,310 bottles of 0.25 mg alprazolam tablets nationwide because the medication was found to be subpotent.

    Product
    ALPRAZOLAM — ALPRAZOLAM (ALPRAZOLAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0873-2015·2014-12-31

    Radiometer HemoCue Glucose 201 Microcuvettes Recalled for Discoloration and Inaccurate Results

    Radiometer America Inc. is recalling HemoCue Glucose 201 Microcuvettes because they show discoloration and provide results outside specification near the end of their shelf life.

    Product
    HemoCue¿ Glucose 201 Microcuvettes, The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201Analyzer and the HemoCue Glucose 201 DM Analyzer (hereafter referred to as the HemoCue Glucose 201 Analyzer). HemoCue Glucose 201 Microcuvettes are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0832-2015·2014-12-31

    Instrumentation Laboratory Recalls HemosIL PT-Fibrinogen HS PLUS Reagent

    Instrumentation Laboratory is recalling HemosIL PT-Fibrinogen HS PLUS reagent kits because some vials exhibit discoloration that causes prolonged prothrombin clotting times.

    Product
    HemosIL PT-Fibrinogen HS PLUS, IVD --- Instrumentation Laboratory IL Company. A high sensitivity thromboplastin reagent based on recombinant human tissue factor (RTF) for the quantitative determination in human citrated plasma of Prothrombin Time (PT) and Fibrinogen on IL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0319-2015·2014-12-31

    Walgreens Aspirin Free Tension Headache Caplets Recalled for Undeclared Sucralose

    LNK International recalled specific lots of Walgreens Aspirin Free Tension Headache Caplets because they contain sucralose, an ingredient not listed on the label.

    Product
    Walgreens ASPIRIN FREE TENSION HEADACHE, Pain Reliever/Pain Reliever Aid, Acetaminophen & Caffeine, 100 Coated Caplets, OTC --- Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, Item # 427594, NDC 0363-0428-12, UPC Code 311917134925
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0839-2015·2014-12-31

    Unapproved Dental Implants Recalled by Instradent USA

    Instradent USA is recalling 13 units of Neodent Titamax WS Cortical Implants because the product is not approved for use in the US.

    Product
    Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous dental implant) Article Number: 109.604 Dental implants are intended for surgical placement in maxillary and/or mandibular arches to provide support for prosthetic restorations in edentulous or partially edentulous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0325-2015·2014-12-31

    Zydus Recalls Benzonatate Capsules Due to Wet or Leaking Defects

    Zydus Pharmaceuticals USA is recalling 19,536 units of Benzonatate capsules because some are wet or leaking. The recall is nationwide.

    Product
    BENZONATATE — BENZONATATE (BENZONATATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0320-2015·2014-12-31

    Sunmark Eye Drops Recalled for Non-GMP API Storage

    K C Pharmaceuticals is recalling Sunmark Eye Drops because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    SUNMARK EYE DROPS ORIGINAL FORMULA — SUNMARK EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0875-2015·2014-12-31

    Zimmer Recalls Trilogy Fiber Metal Acetabular Shell Due to Thread Defect

    Zimmer Manufacturing B.V. is recalling 68 units of Trilogy Fiber Metal Acetabular Shells because the polar-hole threads were found to be undersized, preventing proper attachment to surgical instruments.

    Product
    Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing primary or revision surgery for rehabilitating hips damaged as a result of noninflammatory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0852-2015·2014-12-31

    Getinge 46-Series Medical Washer-Disinfector Recalled for Sediment Residuals

    Getinge Disinfection AB is recalling 46-Series Medical Washer-Disinfector models 46-4 and 46-5 due to sediment residuals in the manifold caused by air pockets.

    Product
    GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 510(k) requirements. For use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0834-2015·2014-12-31

    Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info

    Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.

    Product
    Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Si 3000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0835-2015·2014-12-31

    Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info

    Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.

    Product
    Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Xi 4000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0833-2015·2014-12-31

    GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk

    GE Healthcare is recalling Centricity Enterprise Archive software versions 4.0.x due to a potential data loss issue associated with HL-7 updates.

    Product
    Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. DICOM devices (e..g. modalities, workstations) Communicate with the archive using the DICOM protocol (published by ACR-NEMA). The clinical use is limited to the interaction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0860-2015·2014-12-31

    Siemens ADVIA Centaur XP Immunoassay System Recalled for Tubing Crack Risk

    Siemens Healthcare Diagnostics is recalling 10,515 ADVIA Centaur XP Immunoassay Systems because a slight crack may occur in the tubing at the reservoir connector assembly due to mechanical stress.

    Product
    ADVIA Centaur XP Immunoassay System (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0321-2015·2014-12-31

    KC Pharmaceuticals Recalls Eye Drops Due to Non-GMP API Storage

    KC Pharmaceuticals is recalling 302,976 bottles of Eye Drops A.C. because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    Eye Drops A.C. (Tetrahydrozoline HCl 0.05%, Zinc sulfate 0.25%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Astringent Redness Reliever, Distributed by Safeway Inc., P.O. Box 99, Pleasanton, CA 94566-0009, UPC: 3 21130 70067 8; b) Best Choice, Distributed By: Valu…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0322-2015·2014-12-31

    K C Pharmaceuticals Recalls Eye Drops Due to Warehouse Storage Issues

    K C Pharmaceuticals is recalling specific lots of Eye Drops Industrial Strength because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    Eye Drops Industrial Strength (Polyethylene glycol 400 1%, Tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Manufactured for: Petragon, Inc., Edwardsville, KS 66111; b) SWIFT, Distributed by Swift First Aid, Inc., Valencia, Calif. 91355…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0323-2015·2014-12-31

    KC Pharmaceuticals Recalls Sunmark Eye Drops for CGMP Deviations

    KC Pharmaceuticals is recalling Sunmark Eye Drops Advanced Moisturizer/Lubricant because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT — SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT (DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0318-2015·2014-12-31

    Sulfur8 Medicated Anti-Dandruff Conditioner Recalled for pH Specification Failure

    J. Strickland and Co is recalling Sulfur8 Medicated Anti-Dandruff Conditioner because the product pH failed to meet specifications.

    Product
    sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0313-2015·2014-12-31

    Hospira Recalls Dacarbazine Injection Vials Due to Discoloration

    Hospira Inc. is recalling 3,306 vials of Dacarbazine Injection, USP, 200mg, because the reconstituted solution may appear pink instead of the expected colorless to pale yellow.

    Product
    Dacarbazine, Injection, USP, 200mg, vials packaged in individual cartons, Rx only, Manufactured by Hospira Australia 1 Lexia Place, Mulgrave, Victoria Australia 3170. NDC 61703-327-22.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V827000·2014-12-30

    GM Recalls 2011-2012 Trucks and SUVs for Ignition Lock Defect

    General Motors is recalling 84,192 vehicles because the ignition lock may bind or stick, potentially causing loss of steering and braking power.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, AVALANCHE, SILVERADO, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V826000·2014-12-30

    Dodgen Recalls 2014-2015 RVs for Suspension Tank Bracket Failure Risk

    Dodgen is recalling 2014-2015 Born Free RVs equipped with Liquid Spring suspension kits because a mounting bracket may fail, causing the fluid tank to separate and create a road hazard.

    Product
    DODGEN — DODGEN BORN FREE, BORN FREE MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V829000·2014-12-30

    Spartan Recalls 2015 K3 Chassis Due to Steering Slip Shaft Wear

    Spartan Motors is recalling 32 model year 2015 K3 Chassis vehicles because the steering slip shaft may prematurely wear, increasing the risk of a vehicle crash.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide