The Recall Desk

State

Nebraska product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43626–43650 of 78389

  • SevereFDA (Drugs)·D-0062-2018·2017-11-08

    SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Injection Bags

    SCA Pharmaceuticals is recalling 116 bags of fentanyl and bupivacaine injection due to a lack of assurance of sterility.

    Product
    fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% (Total FentaNYL Dose 500 mcg/250 mL) in 0.9% Sodium Chloride 250 mL Bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205. NDC 70004-0231-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0062-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical ASD Inc. is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., REF 21-7100-24, 100mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plates

    Smiths Medical is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., 50 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps)., REF 21-7001-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0061-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical is recalling CADD Medication Cassette Reservoirs that may have been manufactured with an incorrect pressure plate. The recall covers units distributed worldwide.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer., Nonvented stopper included., 100 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).REF 21-7002-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0057-2018·2017-11-08

    Precision Dose Recalls Subpotent Carbamazepine Oral Suspension Unit Dose Cups

    Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.

    Product
    Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2018·2017-11-08

    AvKARE Recalls Duloxetine Capsules Due to Slightly Elevated Phthalic Acid

    AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.

    Product
    Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2018·2017-11-08

    Teva Recalls Dutasteride and Tamsulosin HCl Capsules for Dissolution Failures

    Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.

    Product
    Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0056-2018·2017-11-08

    Sanofi Recalls Clofarabine Injection Vials Due to Incorrect Package Insert

    Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.

    Product
    Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18025·2017-11-07

    Norco Recalls Children's Bicycles Due to Crank Failure Hazard

    Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.

    Product
    Children's bicycles with Samox cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V702000·2017-11-06

    Crysteel Recalls 2017 Dump Bodies for Driveshaft Detachment Risk

    Crysteel is recalling 2017 dump bodies built on Isuzu NRR-Series chassis because the driveshafts may detach from the rear universal joint, potentially causing loss of propulsion and increasing crash risk.

    Product
    CRYSTEEL — CRYSTEEL DUMP BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V699000·2017-11-06

    Forest River Recalls 2018 Puma Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Puma recreational trailers because the federal placards list incorrect tire size and pressure information, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V700000·2017-11-06

    Triumph Recalls 2016-2017 Speed Triple Motorcycles for Electrical Wiring Defect

    Triumph is recalling 2016-2017 Speed Triple S and R motorcycles because a charging system wire may rub against a bracket, potentially causing an electrical short and engine stall.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE S, SPEED TRIPLE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V696000·2017-11-03

    Jayco Recalls 2016-2018 Jay Flight SLX Trailers Due to Fire Risk

    Jayco is recalling 2016-2018 Jay Flight SLX trailers because the battery circuit lacks overcurrent protection, increasing fire risk during electrical shorts.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V697000·2017-11-03

    Highland Ridge Recalls 2018 Light Trailers Due to Underrated Safety Chains

    Highland Ridge RV is recalling 2018 Light recreational trailers because the safety chains are rated for a lower weight than the trailer's actual capacity, increasing crash risk if detached.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW LIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V695000·2017-11-03

    Entegra Motorhomes Recalled for Missing Exterior Reflectors

    Entegra is recalling 2016-2018 Aspire, Anthem, Cornerstone, and Insignia motorhomes because they lack required reflectors, reducing visibility to other drivers.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·18022·2017-11-02

    Kidde Recalls Fire Extinguishers with Plastic Handles Due to Failure to Discharge

    Kidde is recalling fire extinguishers with plastic handles and Pindicator models because they may fail to discharge or have nozzles detach. One death and 16 injuries have been reported.

    Product
    Kidde fire extinguishers with plastic handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V694000·2017-11-02

    Van-Con Recalls Dual Rear Wheel School Buses Due to Seat Barrier Defect

    Van-Con is recalling 2007-2017 Dual Rear Wheel school buses because the seat barrier behind the driver may be pinned, preventing it from deforming in a crash.

    Product
    VAN-CON — VAN-CON DUAL REAR WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V692000·2017-11-02

    Thor Motor Coach Recalls 2018 Motorhomes Due to Trailer Light Wiring Defect

    Thor Motor Coach is recalling 2018 Ace, Axis, Hurricane, Windsport, and Vegas motorhomes because trailer light wiring may be inserted incorrectly, causing lights to fail and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, AXIS, WINDSPORT, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide