The Recall Desk

State

Nebraska product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41451–41475 of 78321

  • ModerateFDA (Devices)·Z-1462-2018·2018-05-02

    Howmedica Triathlon Revision Knee Implants Recalled for Sizing Errors

    Howmedica Osteonics Corp. is recalling 77 Triathlon Revision Knee implants because customers may receive the incorrect size from what is labeled on the box.

    Product
    Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use devices intended for us in revision total knee arthroplasty to alleviate pain and restore function.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1498-2018·2018-05-02

    Diagnostic Hybrids Recalls MicroVue SC5b-9 Plus EIA Kits Due to Bacterial Contamination

    Diagnostic Hybrids, Inc. is recalling 107 MicroVue SC5b-9 Plus EIA kits because a component was found to contain bacterial contamination.

    Product
    MicroVue SC5b-9 Plus EIA (RUO), Model A020. Research use only (RUO) product. An enzyme immunoassay for the quantitation of SC5b-9 complex present in human plasma or serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0688-2018·2018-05-02

    Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints

    Time-Cap Laboratories is recalling specific lots of Ibuprofen Tablets USP 400 mg due to odor complaints related to CGMP deficiencies.

    Product
    Ibuprofen Tablets USP 400 mg, 500 tablet bottles (NDC 42582-111-18), Rx, Distributed by Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0715-2018·2018-05-02

    McKesson Recalls Diltiazem CD Capsules Due to Dissolution Failures

    McKesson Packaging Services is recalling Diltiazem CD 180 mg capsules because stability testing showed high dissolution results.

    Product
    Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1473-2018·2018-05-02

    Zimmer Biomet Recalls Guide Wires Due to Sterile Packaging Seal Failure

    Zimmer Biomet is recalling Smooth Guide Wire Bullet Tip products because the sterile packaging seal may fail, potentially compromising sterility.

    Product
    Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm Length; Item Number: 47-2255-008-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1485-2018·2018-05-02

    Keystone Dental Recalls Genesis Surgical Cassettes Due to Burr Wobble

    Keystone Dental Inc is recalling 19 Genesis Surgical Cassettes because extra-large grommets cause dental burrs to wobble.

    Product
    Genesis Surgical Cassette Tapered Implants are intended for placement following natural tooth loss or for immediate placement into an extraction socket
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1530-2018·2018-05-02

    Menarini Silicon Biosystems Recalls CellSearch Circulating Tumor Cell Kits

    Menarini Silicon Biosystems is recalling CellSearch Circulating Tumor Cell Kits because unusually high image counts may delay result reporting.

    Product
    CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001) CELLSEARCH¿ CIRCULATING Tumor Cell Kit is intended for the enumeration of circulating tumor cells (CTC) of the epithelial origin (CD45-, EpCAM+, cytokeratins 8, 18+, and/or 19+) in whole blood.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1518-2018·2018-05-02

    CooperVision Clariti 1 Day Contact Lenses Recalled for Incorrect Expiration Date

    CooperVision is recalling specific lots of Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.

    Product
    56% 1 Day Silicone Hydrogel (-2.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of refractiveametropia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0714-2018·2018-05-02

    McKesson Recalls Diltiazem HCl Extended-Release Capsules Due to Dissolution Failures

    McKesson Packaging Services is recalling Diltiazem HCl Extended-Release Capsules because stability testing showed high dissolution results, failing specifications.

    Product
    Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-014-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1517-2018·2018-05-02

    CooperVision Recalls Clariti 1 Day Contact Lenses for Incorrect Expiration Date

    CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.

    Product
    56% 1 Day Silicone Hydrogel (-4.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of refractiveametropia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1515-2018·2018-05-02

    CooperVision Recalls Clariti 1 Day Contact Lenses for Incorrect Expiration Date

    CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.

    Product
    clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1516-2018·2018-05-02

    CooperVision Recalls Clariti 1 Day Contact Lenses for Incorrect Expiration Date

    CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.

    Product
    clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V282000·2018-05-01

    2018 Jeep Cherokee Recalled for Fuel Tube Leak Fire Risk

    Chrysler is recalling 2018 Jeep Cherokee vehicles with 2.4L engines because a fuel tube may leak, increasing the risk of a fire.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V279000·2018-05-01

    2018 Jeep Compass Recalled for Front Suspension Welding Defect

    Chrysler is recalling 2018 Jeep Compass vehicles because front lower control arms may be incorrectly welded, potentially causing separation and loss of vehicle control.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V277000·2018-05-01

    RAM 4500 and 5500 Trucks Recalled for Brake Hose Corrosion Risk

    Chrysler is recalling 2018 RAM 4500 and 5500 trucks because brake hose ferrules may lack anti-corrosion plating, potentially causing fluid leaks and loss of braking.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V280000·2018-05-01

    Chrysler Recalls 2018 Vehicles for Incorrect Transmission Park Lock Rod

    Chrysler is recalling 2018 Dodge, Jeep, Chrysler, and RAM vehicles because an incorrect transmission park lock rod may prevent the vehicle from staying in Park, increasing crash risk.

    Product
    DODGE — DODGE, CHRYSLER, JEEP CHARGER, CHALLENGER, DURANGO, 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V281000·2018-05-01

    Dodge Charger Recall: Front Driveshaft May Detach and Cause Crash

    Chrysler is recalling 2015-2018 Dodge Charger pursuit police vehicles because the front driveshaft may detach, creating a road hazard and increasing crash risk.

    Product
    DODGE — DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18147·2018-05-01

    Sharper Image and Frigidaire Mandoline Slicers Recalled for Laceration Hazard

    Premier Kitchen Products is recalling Sharper Image and Frigidaire mandoline slicers because small blades can separate, posing a laceration hazard. No injuries have been reported.

    Product
    The Sharper Image™ and Frigidaire™ Mandoline slicers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V275000·2018-04-30

    Ford Recalls 2015-2017 Transit Vehicles for Electrical Wiring Fire Risk

    Ford is recalling 25,658 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V276000·2018-04-30

    Altec Heartland Boom-Mounted Saw Recall Due to Valve Adjustment Issue

    Altec is recalling 2017-2018 EC175, EC225, and EC655 Boom-Mounted Saw vehicles because a valve may allow tree trunks to slip or fall, increasing injury risk.

    Product
    ALTEC HEARTLAND — ALTEC HEARTLAND EC225 BOOM-MOUNTED SAW, EC655 BOOM-MOUNTED SAW, EC175 BOOM-MOUNTED SAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·034-2018·2018-04-28

    Pinnacle Foods Recalls Beef Products Due to Possible Processing Deviation

    Pinnacle Foods Inc. is recalling approximately 32,479 pounds of heat-treated, shelf-stable beef products due to a possible processing deviation that may have led to toxin contamination.

    Product
    Pinnacle Foods Inc. Recalls Beef Products Due to Possible Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V272000·2018-04-27

    Mercedes-Benz Recalls SUVs for Active Curve System Fire Risk

    Mercedes-Benz is recalling specific 2012-2017 SUVs because oil in the Active Curve System may leak and cause a fire if the level is low.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GL350, GL450, GL550, AMG GL63
    Category
    Vehicle
    Distribution
    Distributed nationwide