The Recall Desk

State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56201–56225 of 78407

  • SevereNHTSA·15V535000·2015-08-21

    Strick Van Trailer Recall for Suspension Pivot Bolt Failure Risk

    Strick is recalling 2014 Van Trailers with SAF-Holland suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer.

    Product
    STRICK — STRICK VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V534000·2015-08-21

    Chrysler Recalls 2014-2015 Ram 1500 Trucks for Side Air Bag Defect

    Chrysler is recalling 2014-2015 Ram 1500 Quad Cab trucks because side air bag curtains may not fully overlap the C-pillars, increasing injury risk in crashes.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E068000·2015-08-21

    Ricon wheelchair lifts recalled due to potential platform failure

    Ricon is recalling specific wheelchair lifts because oversized pivot holes may allow bearings to shift, potentially causing the platform to fall out of the vehicle.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V532000·2015-08-20

    Oshkosh Recalls 2014-2015 S-Series Concrete Mixers Due to Pressure Relief Defect

    Oshkosh is recalling 2014-2015 S-Series concrete mixers powered by compressed natural gas because pressure relief devices may fail to vent pressure, posing a risk of tank explosion, fire, and injury.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E067000·2015-08-20

    Reyco Granning Recalls Independent Front Suspension Assemblies for Loose Ball Joints

    Reyco Granning is recalling Independent Front Suspension assemblies manufactured between April 2011 and February 2015 due to loose ball joints that could separate and cause a loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V533000·2015-08-20

    Ford Recalls F-650 and F-750 Trucks for Seat Belt Anchor Defect

    Ford is recalling 2011-2013 and 2015 F-650 and F-750 trucks because passenger seat belt anchors may be installed in the wrong location, increasing injury risk in a crash.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2961-2015·2015-08-19

    Bella Rosa Grated Parmesan Cheese Recalled for Undeclared Egg Lysozyme

    Arthur Schuman Inc. is recalling Bella Rosa Grated Parmesan Cheese because it may contain undeclared egg lysozyme, a potential allergen.

    Product
    Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman, Inc. Fairfield, NJ 07064 UPC 088231410041
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1328-2015·2015-08-19

    Methotrexate Injection Recalled Due to Presence of Particulate Matter

    Mylan Institutional LLC is recalling Methotrexate Injection vials due to the presence of particulate matter.

    Product
    Methotrexate Injection, USP 50 mg/2 mL (25 mg/mL), 2 mL Single-dose Vial, packaged in 5 x 2 mL vials per carton, Rx only, labeled as a) Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-0146-01; and b) Manufactured for: Mylan Institutional LLC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2358-2015·2015-08-19

    Invacare Pronto Air Power Wheelchair Recall for Battery Overheating Risk

    Invacare is recalling 1,057 Pronto Air power wheelchairs because the batteries may overheat during charging, posing risks of chemical burns and property damage.

    Product
    Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio, 44035-4190, (800) 333 -6900.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2952-2015·2015-08-19

    D & D Foods Recalls Dijon Mustard Potato Salad for Allergen Mislabeling

    D & D Foods is recalling 110 cases of Dijon Mustard Potato Salad sold in Hy-Vee stores because the product contains milk and wheat but fails to disclose these allergens.

    Product
    Dijon Mustard Potato Salad, NET WT 3 LB (1.36 kg)
    Category
    Food
    Distribution
    8 states
  • SevereCPSC·15748·2015-08-19

    Grizzly Recalls 10-Inch Hybrid Table Saws Due to Laceration Hazards

    Grizzly Industrial is recalling 10-inch hybrid table saws because a loose motor pulley can strike the blade, causing metal fragments to fly and injure users.

    Product
    Grizzly 10-inch hybrid table saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2956-2015·2015-08-19

    FDA Recalls Maxam Products for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all Maxam brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL MAXAM PRODUCTS: The Maxam product is used orally in spray form and bears the Maxam label. ********The List of MAXAM products********************************************** AD Nutritional Support for a Positive Outlook; AFX Nutritional Support for Healthy Cellular…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1329-2015·2015-08-19

    Mylan Recalls Cytarabine Injection Vials Due to Particulate Matter

    Mylan Institutional LLC is recalling 8,340 vials of Cytarabine Injection due to the presence of particulate matter. The affected product was distributed nationwide.

    Product
    Cytarabine Injection 100 mg/5 mL (20 mg/mL), 5 mL Single-Dose Vial (NDC 0069-0152-01), packaged in 10 x 5 mL Vials per carton (NDC 0069-0152-02), Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2373-2015·2015-08-19

    Fresenius Medical Care Recalls Naturalyte Liquid Bicarbonate Concentrate

    Fresenius Medical Care is recalling Naturalyte Liquid Bicarbonate Concentrate due to potential bacterial contamination. The recall covers 2,264,028 units distributed nationwide.

    Product
    Naturalyte Liquid Bicarbonate Concentrate 6.4 liter bottle A Dialysate Concentrate for Hemodialysis (liquid) Product Code: 08-4000-LB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V531000·2015-08-19

    Thor Motor Coach Recalls Tuscany XTE Motorhomes for Table Defect

    Thor Motor Coach is recalling 2014-2015 Tuscany XTE motorhomes because the dinette table insert may flip up if sat on, posing a fall risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY XTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2366-2015·2015-08-19

    Hitachi Oasis MRI Coil Extension Cable Recalled for Overheating Burn Hazard

    Hitachi Medical Systems America Inc is recalling 173 Oasis Coil Extension Cables used with MRI systems because they may overheat and cause burns.

    Product
    Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2356-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia SD, User Manual #1400191. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2350-2015·2015-08-19

    Remel Recalls PathoDx Strep Grouping Kits Due to Reagent Issues

    Remel Inc is recalling 1,859 PathoDx Strep Grouping Kits because a reagent may cause weak reactions, potentially leading to failure to identify target species.

    Product
    PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2357-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia HD, User Manual #1513140. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2355-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Spring Arm Defect

    Trumpf Medical Systems is recalling 9,287 ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2946-2015·2015-08-19

    Novacare Recalls Glucosamine Capsules Due to Inadequate Allergen Labeling

    Novacare, LLC is recalling 961 bottles of Glucosamine 750 mg capsules nationwide because the product has inadequate allergen labeling.

    Product
    Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V530000·2015-08-19

    Thor Motor Coach Recalls 2016 Vegas and Axis RVs for HVAC Defect

    Thor Motor Coach is recalling 290 model year 2016 Vegas and Axis recreational vehicles because the HVAC control may lock, preventing windshield defrosting and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VEGAS, AXIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2957-2015·2015-08-19

    ASN Dietary Supplements Recalled for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label. *********the List of ASN products***************************** AFINITY WHEY PROTEIN; DHEA; HUMAGRO Homeopathic Growth Hormone 4c; PHYTOBOL; TESTRX; TRIBESTRONE II;
    Category
    Drug
    Distribution
    Distributed nationwide