The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48251–48275 of 78397

  • HighFDA (Devices)·Z-0885-2017·2016-12-28

    Siemens IMMULITE 2000 PSA Assay Recalled for Hook Effect Performance Issues

    Siemens Healthcare Diagnostics is recalling IMMULITE 2000 PSA assays because they do not meet the High-dose Hook Effect expectations stated in the Instructions for Use.

    Product
    IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number L2KPTS2, SMN 10706281 and REF/Catalog Number L2KPTS6, SMN 10706282 (US); REF/Catalog Number L2KPS2, SMN 10380986 and REF/Catalog Number L2KPS6, SMN 10380996 (OUS); IVD --- Origin…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0775-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 996 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970515, Catalog No.REF 06597051, 2) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970535, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0829-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Brown Sugar Style Smoked Black Cod Black Cod, **Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0777-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 7 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach from the hub during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO B PG, Item Number H787065970685, Catalog No.REF 06597068, 2) 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO S PG, Item Number H787065970705…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0825-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because the products contain undeclared soy.

    Product
    PREMIUM SMOKED SALMON***CAJUN***NET WT: 4OZ***Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee. UPC 7 02772 00562 6.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0823-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    WILD CATCH PREMIUM SMOKED SALMON***NATURAL***NET WT: 4OZ*** UPC 7 02772 00559 6. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0773-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Component Defect

    AngioDynamics is recalling 80 boxes of Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO B PG, Item Number H787065970465, Catalog No.REF 06597046, 2) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO S PG, Item Number H787065970485, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0884-2017·2016-12-28

    Siemens IMMULITE PSA Assay Recalled for High-Dose Hook Effect Failure

    Siemens Healthcare Diagnostics is recalling IMMULITE PSA assays because they do not meet the high-dose hook effect expectations stated in the Instructions for Use.

    Product
    IMMULITE/IMMULITE 1000 Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number LKPTS1, Siemens Material Number (SMN) 10706279 (US); Catalog Number LKPS1, SMN 10380960 and Catalog Number LKPS5, SMN 10380949 (OUS); IVD --- Origin: UK Siemens Healthcare Diagnostics…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2017·2016-12-28

    Medtronic Recalls Clearify Visualization Systems Due to Sterility Compromise

    Medtronic is recalling 230 Clearify Visualization Systems because the sterile barrier was breached, compromising product sterility. The recall covers worldwide distribution.

    Product
    Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0778-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 4F Stiffened Micro-Introducer Kits because the sheath/dilator components may have a rotating luer that detaches from the hub during use.

    Product
    ANGIODYNAMICS 4F Stiffened Micro-Introducer, Item Number H787065971035, Catalog No.REF 06597103 Indicated for percutaneous introduction of guidewire or catheter into the vascular system following a small 21-gauge needle stick
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0826-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    PREMIUM SMOKED SALMON UPC 7 02772 00564 0 Packaged in a 5 lb case 20/4oz vacuum packaged per case. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0810-2017·2016-12-28

    Brownwood Farms Recalls Yankee Bourbon BBQ Sauce for Undeclared Soy

    Brownwood Farms is recalling Yankee Bourbon BBQ Sauce because it contains soy ingredients not declared on the label.

    Product
    Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottles and 1 gallon
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0776-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 145 boxes of Stiffened Micro-Introducer Kits because the sheath/dilator components may have a rotating luer that detaches during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T NON-ECHO S PG, Item Number H787065970655, Catalog No.REF 06597065, 2) 4 F Stiffened Micro-Introducer Kit, STF 4F M.I. KIT 45CM NT/T NON-ECHO S PG, Item Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2017·2016-12-28

    Teleflex Recalls Mucosal Atomization Devices Due to Incomplete Atomization

    Teleflex Medical is recalling Mucosal Atomization Devices because they may produce a straight stream instead of a fully atomized plume of medication.

    Product
    Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code MAD100, MAD100OS MAD110, MAD110OS, MAD130, MAD130OS, MAD140, MAD140OS, MAD300, MAD300B. Manufactured By: Wolfe-Tory Medical, Inc., Teleflex Medical. For…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0831-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Smoked Trout Rainbow Trout, NORTHERN FISH PRODUCTS, INC.***" Packaged in bulk 10lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0821-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy. The recall excludes hot jerky salmon and jerky salmon.

    Product
    "***NORTHERN CLASSICS NATURAL SMOKED SALMON. Net WT. is filled in on a separate white label. Product is frozen and vacuum packed. Product also referred to as SALMON HOT SMKD SIDE ATL SK-ON.
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·16V938000·2016-12-28

    Navistar Recalls 2017 International Trucks Due to Battery Latch Fire Risk

    Navistar is recalling 2017 International ProStar, LoneStar, 9900i, and TranStar trucks because a battery latch may cause an electrical short and fire.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, 9900I, TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0824-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Fish for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    ***NORTHERN CLASSICS FINEST QUALITY KIPPERED SALMON CHUNKLETS. This package can be combined with other products and placed into a combination package. Each package is individually labeled. Bulk cases contain 5 lbs.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0784-2017·2016-12-28

    Ultroid Procedure Pack Recalled for Quality System Non-Compliance

    Ultroid Technologies is recalling 52,084 procedure packs because they were not manufactured under required quality system controls.

    Product
    Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-0877-2017·2016-12-28

    BD SurePath Collection Vials Recalled Due to Cracked Caps

    Becton Dickinson is recalling SurePath collection vials because cracked caps may allow preservative fluid to leak.

    Product
    BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed for use with the PrepStain¿ System. SurePath¿ Preservative Fluid is an alcohol-based, preservation solution that serves as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0774-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 751 Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970505, Catalog No.REF 06597050, 2) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970525, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide