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.

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.

59301–59325 of 78413

  • SevereNHTSA·15V046000·2015-01-28

    Chrysler Recalls Jeep and Dodge Vehicles for Air Bag Defect

    Chrysler is recalling specific 2002-2004 Jeep and Dodge vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    JEEP — JEEP, DODGE LIBERTY, GRAND CHEROKEE, VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0379-2015·2015-01-28

    Valeant Recalls Virazole Due to Microbial Contamination

    Valeant Pharmaceuticals is recalling Virazole (ribavirin) inhalation solution due to positive microbial contamination found during stability testing.

    Product
    Virazole (Ribavirin for Inhalation Solution, USP), Sterile Lyophilized For Administration by Aerosol Inhalation Only, Rx only, Contents: Four 6 g vials, 100 mL, Distributed by: Valeant Pharmaceuticals North America, Bridgewater, NJ 08807 USA, NDC 0187-0007-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0377-2015·2015-01-28

    Mylan Recalls Ciprofloxacin Tablets Due to Manufacturing Deviations

    Mylan Institutional, Inc. is recalling Ciprofloxacin Tablets 500 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.

    Product
    CIPROFLOXACIN TABLETS, USP, 500 mg, 100 Tablets (10 tablets per blister card. 10 blister cards per carton), Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 51079-182-20.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1003-2015·2015-01-28

    Dick's Sporting Goods Recalls Fitness Gear Inversion Tables Due to Injury Reports

    Dick's Sporting Goods is recalling Fitness Gear Inversion Tables because customers reported falling and sustaining injuries. The products were distributed nationwide.

    Product
    Fitness Gear Inversion table (Style STE00059FG or Style STE00118FG), Distributed by ASLI, Wilmington, DE (on carton), Paradigm Health & Wellness, Inc. (in user manuals); The products are inversion tables, which allow the user to secure his or her ankles to the table and invert.…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0923-2015·2015-01-28

    Roland Bruschetta Recalled Due to Glass Fragment Contamination

    American Roland Food Corp. is recalling Roland brand Bruschetta, Italian-Style Appetizer, because glass fragments were found in the product.

    Product
    Roland brand Bruschetta, Italian-Style Appetizer, NET WT. 12 OZ. (340g), Item 46740, UPC 41224467408, PRODUCT OF TURKEY ---The product is packaged in a glass jar, 12 x 12 oz. jars per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V045000·2015-01-28

    Honda Recalls 2003-2004 Odyssey and 2003 Acura MDX for Air Bag Defect

    Honda is recalling 2003-2004 Odyssey and 2003 Acura MDX vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    HONDA — HONDA, ACURA ODYSSEY, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2015·2015-01-28

    Maquet Tegris System Recalled Due to Software Error in Operating Table Commands

    Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.

    Product
    TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V040000·2015-01-28

    Ford Recalls Taurus and Lincoln MKS for Door Handle Spring Defect

    Ford is recalling 2010-2013 Taurus and 2011-2013 Lincoln MKS vehicles because an interior door handle spring may unseat, preventing the handle from returning to its stowed position.

    Product
    FORD — FORD, LINCOLN TAURUS, MKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1000-2015·2015-01-28

    BD Biosciences Recalls Contaminated CD8 PE In Vitro Diagnostic Reagent

    BD Biosciences is recalling one lot of CD8 PE reagent contaminated with CD4 FITC, which may cause incorrect patient data.

    Product
    CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340046. Hematology: Single color direct immunofluorescence reagent for enumerating percentages of mature human suppressor/cytotoxic (CD8+) lymphocytes in erythrocyte-lysed whole blood or peripheral blood mononuclear cell…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0998-2015·2015-01-28

    Cordis POWERFLEX PRO PTA Dilatation Catheter Recall for Unsterilized Unit

    Cordis Corporation is recalling one unsterilized unit of the POWERFLEX PRO PTA Dilatation Catheter from a demonstration lot left at a hospital.

    Product
    Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1002-2015·2015-01-28

    BD Biosciences Recalls Contaminated Anti-Lambda APC-H7 Antibody Lots

    BD Biosciences is recalling two lots of Anti-Lambda APC-H7 antibody due to contamination with CD38 antibody. The product is used for in vitro flow cytometric immunophenotyping.

    Product
    Anti-Lambda APC-H7, Catalog Number 656157. Product Usage: Intended for in vitro flow cytometric immunophenotyping of hematologic disorders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0378-2015·2015-01-28

    Mylan Lamotrigine Tablets Recalled for CGMP Deviations

    Mylan Institutional is recalling 3,993 cartons of Lamotrigine 200 mg tablets because they were not manufactured according to Good Manufacturing Practices.

    Product
    LAMOTRIGINE TABLETS, 200 mg, 100 Tablets (10 tablets per blister card x 10 blister cards per carton), Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 51079-866-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2015·2015-01-28

    Genetic Testing Institute Recalls PF4 Concentrated Wash Reagent Lots

    Genetic Testing Institute is recalling specific lots of PF4 Concentrated Wash (10x) because the reagent is slightly more dilute than intended, which may cause false positive test results.

    Product
    PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG (catalog numbers HAT13G, HAT45G) and 2. ImmucorGamma LIFECODES PF4 Enhanced (catalog numbers X-HAT13, X-HAT45) The PF4 IgG assay is an Enzyme Linked…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1006-2015·2015-01-28

    Aptalis Flutter Percussor Respiratory Device Recalled for Packaging Defect

    Aptalis Pharmatech Inc. is recalling approximately 49,000 Flutter Percussor respiratory devices because the packaging may be difficult to open or close.

    Product
    FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a percussor device, intended to be used as a mucus clearance device for patients with mucus producing respiratory conditions such as: atelectasis, bronchitis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0376-2015·2015-01-28

    3M ESPE Clinpro 5000 Toothpaste Recalled for Missing Lot and Expiration Dates

    3M ESPE is recalling 19,728 tubes of Clinpro 5000 Anti-Cavity Toothpaste because the primary boxes are missing lot numbers and expiration dates.

    Product
    3M ESPE Clinpro 5000 (1.1% Sodium Flouride), Anti-Cavity Toothpaste, 4 oz tube (NDC 48878-3130-04), Rx Only, Manufactured for 3M ESPE Dental Products, St. Paul, MN 55144
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V039000·2015-01-27

    Land Rover Recalls Range Rovers Due to Brake Hose Rupture Risk

    Jaguar Land Rover is recalling 2006-2012 Range Rovers because front brake hoses may rupture, causing loss of brake fluid and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V038000·2015-01-27

    Jaguar Recalls 2012-2015 XK Models for Front Side Lamp Defect

    Jaguar is recalling 2012-2015 XK vehicles because front side lamps may turn off after five minutes, reducing visibility and increasing crash risk.

    Product
    JAGUAR — JAGUAR XK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V036000·2015-01-27

    Peterbilt 389 Recall for Electronic Stability Control Sensor Defect

    PACCAR is recalling 2015 Peterbilt 389 trucks because an incorrect horn contact plate may damage the ESC steering angle sensor, increasing crash risk.

    Product
    PETERBILT — PETERBILT 389
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15064·2015-01-27

    Mirka Recalls Compact Electric Random Orbital Sanders Due to Fire Hazard

    Mirka Abrasives is recalling specific 5-inch and 6-inch compact electric random orbital sanders because they can short circuit, posing a fire hazard. No injuries or property damage have been reported.

    Product
    Random orbital sanders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V037000·2015-01-27

    Jaguar Recalls 2015 XJ Models for Incorrect Air Bag Manual Description

    Jaguar is recalling 1,346 model year 2015 XJ vehicles because the owner's manual incorrectly describes the Occupant Sensor System, potentially increasing injury risk in a crash.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V035000·2015-01-27

    Crossroads Recalls 2015 Z1 Trailers Due to Incorrect Ramp Load Labels

    Crossroads RV is recalling 2015 Z1 toyhauler trailers because the front loading ramps display a 700-pound capacity limit, but the actual limit is 500 pounds.

    Product
    CROSSROADS — CROSSROADS Z1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·021-2015·2015-01-26

    Oscar's Hickory House Recalls Sausage for Undeclared Allergens

    Oscar's Hickory House is recalling approximately 376 pounds of sausage products due to misbranding and undeclared allergens, including soy, milk, wheat, and sulfites.

    Product
    Oscar's Hickory House Inc. — New York Firm Recalls Sausage Products Due to Misbranding and An Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide