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.

57701–57725 of 78413

  • ModerateFDA (Devices)·Z-1532-2015·2015-05-06

    Beckman Coulter Recalls MicroScan Dried Gram Negative MIC Panels

    Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis and Imipenem.

    Product
    MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20 Breakpoints Panel: Neg/Urine Combo 61, Catalog B1017-414 Microbiology: For use with MicroScan Dried Gram Negative MIC/Combo Panels and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1524-2015·2015-05-06

    Beckman Coulter Recalls MicroScan Pos Combo 33 Panels Due to Missing Desiccants

    Beckman Coulter is recalling 664 boxes of MicroScan Pos Combo 33 panels because some were packaged without desiccants, which may cause substrate deterioration.

    Product
    MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 MicroScan Pos Combo 33 B1017-211 panels are designed for use in determining quantitative and /or qualitative antimicrobial agent susceptibility and/or identification to the species level of colonies, grown…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1535-2015·2015-05-06

    Biocare Medical Recalls CD99 In Vitro Diagnostic Reagent Lots

    Biocare Medical is recalling specific lots of CD99 in vitro diagnostic reagents because staining intensity has decreased over time, potentially affecting shelf life.

    Product
    CD99 Catalog number PM008 AA; For In Vitro Diagnostic Use. Product Usage: Provides adjunctive diagnostic information following the primary diagnosis of a neoplasm by conventional histopathology methods.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1540-2015·2015-05-06

    Therasage FAR-Infrared Heat Home Sauna Recalled for Lack of FDA Approval

    Therasage, LLC. is recalling FAR-Infrared Heat Home Saunas because they were distributed without FDA 510(k) approval.

    Product
    FAR-Infrared Heat Home Sauna, 3 person Indications including, but not limited to Natural pain relief, Negative ion therapy , Heart Health, Cancer Therapy, Lyme Disease, and ... to reduce neurosis and anxiety .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1544-2015·2015-05-06

    Integra Tuohy Needles Recalled for Incorrect Length Labeling

    Integra LifeSciences is recalling 90 Tuohy needles that were incorrectly labeled as 5 inches when they are actually 3.5 inches.

    Product
    Integra Long Epidural Steroid Injection Needle (Tuohy Needle), 18 Gauge x 5 inch Removable Wing, Metal Stylet, Calibrations (10BX), Catalogue No. PITRW1850. Used to administer steroid medication in the epidural space.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1550-2015·2015-05-06

    Fresenius 2008T Hemodialysis Machines Recalled for Acetate Display Error

    Fresenius Medical Care is recalling 2008T hemodialysis machines because the Select Concentrate screen incorrectly displays the GranuFlo acetate value as 4mEq/l instead of 8mEq/l.

    Product
    2008 Series Hemodialysis Machines: 2008T with the following product code and description: 190395 2008K at Home System - 1st Gen. -¿ Canada; 190828 2008K at Home System - 2nd Gen - U.S.; 190904 2008K at Home System w/ Bibag; 190828 2008KatHOME HEMODIALYSIS SYSTEM; 190395…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1541-2015·2015-05-06

    Therasage Portable FAR Infrared Sauna Recalled for Lack of FDA Approval

    Therasage, LLC. is recalling 8 portable FAR infrared saunas because they were distributed without FDA 510(k) approval.

    Product
    Portable FAR Infrared Sauna Indications including, but not limited to Natural pain relief, Negative ion therapy , Heart Health, Cancer Therapy, Lyme Disease, and ... to reduce neurosis and anxiety .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1522-2015·2015-05-06

    Beckman Coulter Recalls MicroScan Neg Breakpoint Combo Panel Type 34

    Beckman Coulter is recalling 681 boxes of MicroScan Neg Breakpoint Combo Panel Type 34 due to reported panel degradation.

    Product
    MicroScan -Neg Breakpoint Combo Panel Type 34; Catalog number B1017-404; Panel MicroScan Neg Breakpoint 34 Neg panels are designed for use in determining quantitative and /or qualitative antimicrobial agent susceptibility and /or identification to No.1 the species level of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1558-2015·2015-05-06

    Teleflex Medical Recalls Hudson RCI ConchaTherm Neptune Heated Humidifiers

    Teleflex Medical is recalling 7,228 Hudson RCI ConchaTherm Neptune Heated Humidifiers because customer complaints reported the power ceasing and the display going blank.

    Product
    Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1531-2015·2015-05-06

    Beckman Coulter Recalls MicroScan Microbiology Panels Due to Performance Limitation

    Beckman Coulter is recalling MicroScan Microbiology Systems panels because a 2013 bulletin failed to mention a performance limitation for Proteus mirabilis and Imipenem.

    Product
    MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20 Breakpoints Panel: Neg/Urine Combo 55, Catalog B1017-409 Microbiology: For use with MicroScan Dried Gram Negative MIC/Combo Panels and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1549-2015·2015-05-06

    Fresenius 2008 Hemodialysis Machines Recalled for Acetate Display Error

    Fresenius Medical Care is recalling 2008 Series Hemodialysis Machines because the Acetate value for GranuFlo is displayed incorrectly on the Select Concentrate screen.

    Product
    2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 BIBAG WITHOUT CDX; 190908 2008T HD SYSTEM WITH CDX, CANADA; 190713 2008T HEMODIALYSIS SYS., with CDX; 190766 2008T HEMODIALYSIS SYSTEM W/BIBAG; 190858 2008T HEMODIALYSIS SYSTEM WITHOUT CDX The Fresenius 2008K…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1533-2015·2015-05-06

    Beckman Coulter Recalls MicroScan Dried Gram Negative MIC Panels

    Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis and Imipenem.

    Product
    MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20 Breakpoints Panel: Neg MIC 38, Catalog B1017-412 Microbiology: For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1537-2015·2015-05-06

    GA Industries Recalls Logicon Caries Detector for Lack of FDA Approval

    GA Industries is recalling the Logicon Caries Detector software because it was released without FDA approval.

    Product
    Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces for decay using digital radiographs. -Initial radiographic assessment of inter-proximal caries (Presently limited to RVG 6100 & 6500 bitewing radiographs in horizontal format)  Identify and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V261000·2015-05-05

    Mercedes-Benz Recalls 2015 Sprinter Vehicles Due to Oil Leak Fire Risk

    Mercedes-Benz is recalling 2015 Sprinter 2500 and 3500 vehicles because oil may leak from the chain tensioner gasket, posing a fire and road hazard risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V264000·2015-05-05

    Eldorado Amerivan 10 Recall for Rear Shock Absorber Separation Risk

    Eldorado is recalling 2012-2015 Amerivan 10 vehicles because the rear shock absorber may separate, potentially damaging fuel lines and causing a fire.

    Product
    ELDORADO — ELDORADO AMERIVAN 10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V262000·2015-05-05

    Gillig Low Floor Vehicles Recalled for Engine Oil Fire Risk

    Gillig is recalling 2010-2015 Low Floor vehicles because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V259000·2015-05-04

    Jayco Eagle Fifth Wheel Trailer Recall for Wheel Stud Defect

    Jayco is recalling 2016 Eagle fifth wheel trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E033000·2015-05-04

    Vapor Bus Recalls ETO Controller Assemblies Due to Software Defect

    Vapor Bus is recalling ETO Controller Assemblies because a software defect may cause rear passenger doors to open without warning while the bus is moving.

    Product
    ELECTRICAL SYSTEM:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V260000·2015-05-04

    Eldorado Passport HD Recall: Power Cable Chafing May Cause Fire

    Eldorado National is recalling 2012-2014 Passport HD vehicles because a power cable may chafe and short, increasing the risk of a fire.

    Product
    ELDORADO — ELDORADO PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V258000·2015-05-01

    Starcraft RV Recalls 2016 Travel Trailers with Incorrect Tire Labels

    Starcraft RV is recalling 36 model year 2016 Launch and AR-One travel trailers because Federal Certification Labels may list the wrong tire size.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE, LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V257000·2015-05-01

    Holiday Rambler Fifth Wheel Trailers Recalled for Microwave Fire Risk

    Allied Recreation Group is recalling specific Holiday Rambler fifth wheel trailers because the installed microwaves may start on their own, posing a fire hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER PRESIDENTIAL, ALUMASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide