The Recall Desk

State

Nebraska product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52801–52825 of 78404

  • ModerateFDA (Food)·F-0814-2016·2016-04-06

    Ventura Foods Recalls Canola Frying Oil Due to Plastic Contamination

    Ventura Foods is recalling 35 lb. jugs of canola frying oil because plastic from the jug's sealing surface may have been pushed into the product during manufacturing.

    Product
    18159-BLN : Brilliance Clear Zero Premium Clear Canola Frying Oil 35 lb. ; 58503-CHP : Chef's Pride Canola Clear Fry Oil 35 lb. ; 58503-FLV : Flavorite Canola Clear Fry Oil 35 lb. ; 58503-PLF : Planet Fry Canola Clear Fry Oil 35 lb. ; 58503-NGT : Nugget Brand Canola Clear…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1279-2016·2016-04-06

    Philips MultiDiagnost Eleva Foot Switches Recalled for Bent Pedal Defect

    Philips Medical Systems is recalling 168 foot switches used with the MultiDiagnost Eleva system because a bent pedal can cause loss of key image functionality.

    Product
    Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 This Philips MultiDiagnost Eleva is intended to be used as a multifunctional/universal system. General RIF, Fluoroscopy, Radiography and Angiography can be performed along with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1001-2016·2016-04-06

    ProSupps Recalls Mr. Hyde Pre-Workout for Undeclared Picamilon Ingredient

    ProSupps USA LLC is recalling 33 units of Mr. Hyde Intense Energy Pre-Workout because the product may contain undeclared Picamilon.

    Product
    Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS BLUERAZZ NATURAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 3.7 OZ (105 GRAMS) packaged in red plastic jars with black lids.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1252-2016·2016-04-06

    Molteno3 Glaucoma Implants Recalled for Updated Instructions

    Innovative Ophthalmic Products is recalling Molteno3 Glaucoma Implants because the package insert was updated to add a caution statement to minimize off-label use.

    Product
    Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#: M3-175) GL-Single Plate 230mm2 (IOP reorder#: M3-230)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1268-2016·2016-04-06

    Pelton & Crane Recalls Helios Track Mounted Dental Lights

    Pelton & Crane is recalling 156 Helios HL3T and HLT track mounted dental lights because they were missing two set screws during initial installation.

    Product
    Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1264-2016·2016-04-06

    Wfr/aquaplast Recalls Prone Breast Treatment Tables Due to Scale Misalignment

    Wfr/aquaplast Corp is recalling 30 prone breast treatment tables and devices because some may have misaligned scales, potentially causing orientation differences.

    Product
    Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device Product Usage: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device is a medical charged-particle radiation therapy system. A breast radiation therapy patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1285-2016·2016-04-06

    Ossur Recalls Knee Shields and Medical Devices Due to Packaging Defect

    Ossur Americas is recalling various medical devices, including knee shields and walkers, because the packaging is defective.

    Product
    Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide protection from debris or impact to the patella while a patient participates in motocross activities.
    Category
    Medical Device
    Distribution
    48 states
  • LowFDA (Drugs)·D-0783-2016·2016-04-06

    Praxair Recalls Medical Air Cylinders Due to Odor Complaint

    Praxair Inc. is recalling 382 cylinders of medical air nationwide after a customer reported an odor when turning on a cylinder.

    Product
    UN1002 Air, Compressed, Medical Air, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0800-2016·2016-04-06

    Pfizer Recalls Robitussin Peak Cold Liquid Due to Labeling Error

    Pfizer is recalling 63,636 bottles of Robitussin Peak Cold Liquid nationwide due to a label mix-up. Consumers should stop using the product and return it to the point of purchase.

    Product
    Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V190000·2016-04-05

    Hyundai Recalls 2011 Sonata Vehicles for Power Steering Defect

    Hyundai is recalling 2011 Sonata vehicles because a damaged circuit board may cause a loss of power steering assist, increasing the risk of a crash.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16736·2016-04-05

    Givenchy Recalls Men's Silk T-Shirts for Flammability Violation

    Givenchy is recalling about 60 men's silk T-shirts because they fail to meet federal flammability standards, posing a risk of burn injury.

    Product
    Givenchy men's silk T-shirts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E027000·2016-04-05

    Hale Recalls 6 Inch Suction Strainers Due to Soldering Defect

    Hale Products Inc. is recalling 6 Inch Suction Strainers manufactured between July 2015 and March 2016. Improper soldering may cause the strainer to break, potentially damaging fire pumps and increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V191000·2016-04-05

    Nova Bus Recalls 2010-2015 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2010-2015 LFS transit buses because missing welds on seat J-Brackets may allow seat belt anchorages to separate, increasing injury risk in a crash.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V189000·2016-04-04

    Kalmar Ottawa T2 Recalled for Inaccurate Brake Pressure Gauge

    Kalmar is recalling 2014-2016 Ottawa T2 vehicles because the brake system air pressure gauge may not display accurate levels, increasing crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E026000·2016-04-01

    Bosch Recalls Aftermarket Brake Pads for Ford, Lincoln, and Mercury Vehicles

    Bosch is recalling specific aftermarket front brake pads for 1993-2007 Ford, Lincoln, and Mercury vehicles because a shifting shim may damage the brake disc, potentially reducing braking power.

    Product
    FORD — FORD, LINCOLN, MERCURY TAURUS, TAURUS SHO, CONTINENTAL, SABLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V185000·2016-04-01

    Kompact Kamp Recalls Motorcycle Trailers Missing Side Marker Lights

    Kompact Kamp is recalling 1983-2016 Li'l Clipper motorcycle trailers manufactured without side marker lights, which may decrease visibility and increase crash risk.

    Product
    KOMPACT KAMP — KOMPACT KAMP LI'L CLIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V186000·2016-04-01

    Pierce Recalls 2010-2016 Vehicles Due to Flashlight Battery Fire Risk

    Pierce Manufacturing is recalling 2010-2016 Arrow-XT, Quantum, and Velocity vehicles because Pelican flashlights may overheat and cause a fire.

    Product
    PIERCE — PIERCE VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V183000·2016-03-31

    Ford Recalls 2015-2016 Lincoln MKC and Explorer for Fire Risk

    Ford is recalling 2015-2016 Lincoln MKC and 2016 Ford Explorer vehicles because engine block heaters may overheat and cause a fire.

    Product
    LINCOLN — LINCOLN, FORD MKC, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E024000·2016-03-31

    Strategic Sports Recalls Leather Up XElement Motorcycle Helmets

    Strategic Sports is recalling specific Leather Up XElement motorcycle helmets that may not adequately protect users in a crash, failing federal safety standards.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide