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.

56176–56200 of 78407

  • ModerateFDA (Devices)·Z-2384-2015·2015-08-26

    C.R. Bard Recalls Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters

    C.R. Bard is recalling 14,310 units of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.

    Product
    Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2420-2015·2015-08-26

    Medtronic EOPA Arterial Cannula Recalled for Missing Guidewire

    Medtronic is recalling EOPA Arterial Cannulas (Lot 2015060544) because they were shipped without the required guidewire.

    Product
    Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2422-2015·2015-08-26

    International Biophysics Recalls IBC Suction Wands Due to Seal Defects

    International Biophysics Corp. is recalling 100 IBC Suction Wands because heat seals on sterile pouches may not meet strength criteria.

    Product
    IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Suction Wand is a component of Blood Recovery System for use in open heart procedures, autologous blood recovery and blood suction. It is a disposable, single use component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2421-2015·2015-08-26

    Trilliant Surgical Recalls Non-Sterile Cannulated Screw Countersinks

    Trilliant Surgical Ltd. is recalling 102 units of non-sterile cannulated screw countersinks because their cutting efficiency was out of specification.

    Product
    2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part # 210-40-002 NON-STERILE Product Usage: The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2424-2015·2015-08-26

    International Biophysics Corp. Recalls IBC Vascular Loops Due to Seal Issues

    International Biophysics Corp. is recalling 771 IBC Vascular Loops because heat seals on sterile pouches may not meet strength criteria.

    Product
    IBC Vascular Loop Catalog Number CH111, CH112, CH113, CH114, CH115, CH116, CH118 Product Usage: The IBC Vascular Loop is a single-use, disposable loop used in occluding, retracting, and identifying arteries, veins, tendons, and nerves in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1346-2015·2015-08-26

    Wockhardt Recalls Lisinopril Tablets Due to Inadequate Complaint Investigations

    Wockhardt USA is recalling 1,704 bottles of Lisinopril 5 mg tablets because an FDA inspection found inadequate investigations of past market complaints.

    Product
    Lisinopril Tablets USP, 5 mg, 1000-count bottles, Rx Only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054 USA, UPC 3 64679 92806 6, NDC 64679-928-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2416-2015·2015-08-26

    Siemens ADVIA Chemistry Acetaminophen Reagents Recalled for NAC Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Acetaminophen reagents due to a change in N-acetylcysteine concentration that may cause assay interference.

    Product
    ADVIA Chemistry Acetaminophen reagents; for in vitro diagnostic use in the quantitative determination of acetaminophen in human serum and plasma (lithium heparin) on ADVIA Chemistry systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1348-2015·2015-08-26

    UCB Recalls Univasc Tablets Due to Failed Dissolution Testing

    UCB, Inc. is recalling Univasc (moexipril HCl) tablets because they failed 24-month dissolution testing. The recall covers 2,916 bottles distributed nationwide.

    Product
    univasc (moexipril HCl) tablets, 7.5 mg, 100 Ct Bottle, Rx Only. Manufactured for UCB, Inc., Smyrna, GA 30080. NDC: 0091-3707-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2387-2015·2015-08-26

    C.R. Bard Recalls Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters

    C.R. Bard is recalling specific lots of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.

    Product
    Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 16 Fr, (30/box), Product Code 51616. Intermittent catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2386-2015·2015-08-26

    C.R. Bard Recalls Magic3 Female Intermittent Urinary Catheters

    C.R. Bard is recalling 37,686 Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.

    Product
    Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 14 Fr, (30/box), Product Code 51614. Intermittent catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2432-2015·2015-08-26

    Cepheid Recalls Xpert CT/NG Urine Specimen Collection Kits

    Cepheid is recalling Xpert CT/NG Urine Specimen Collection Kits because some lots contain a sub-component with an expiration date earlier than the kit's expiration date.

    Product
    Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50; Microbiology: Xpert CT/NG Urine Specimen Collection Kit is designed to preserve and transport Chlamydia trachomatis and Neisseria gonorrhoeae DNA in first-catch male and female urine specimens from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2431-2015·2015-08-26

    Cepheid Recalls Xpert CT/NG Vaginal and Endocervical Specimen Collection Kits

    Cepheid is recalling Xpert CT/NG Vaginal/Endocervical Specimen Collection Kits because some lots contain a sub-component with an earlier expiration date than the kit itself.

    Product
    Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number CT/NGSWAB-50; Microbiology: The Cepheid X pert CT /NG Vagina Endocervical/ Specimen Collection Kit is designed to collect, preserve and transport patient Chlamydia trachomatis and Neisseria gonorrhoeae…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1345-2015·2015-08-26

    Sun Pharma Recalls Bupropion Hydrochloride Tablets for Dissolution Failure

    Sun Pharma Global Fze is recalling 35,235 bottles of Bupropion Hydrochloride Extended-Release Tablets because they failed to meet drug release specifications during stability testing.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·15749·2015-08-25

    Cybex Recalls Arm Curl Machines Due to Impact Injury Hazard

    Cybex International is recalling about 4,400 arm curl machines because swivel handles can break off, posing an impact injury hazard to users.

    Product
    Arm Curl Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15222·2015-08-25

    Scag Liberty-Z Lawn Mowers Recalled for Gas Tank Fire Hazard

    Scag Power Equipment is recalling about 4,400 Liberty-Z zero-turn lawn mowers because the gas tank can leak, posing a fire hazard. No injuries have been reported.

    Product
    Scag Liberty-Z zero-turn lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·113-2015·2015-08-25

    Kraft Heinz Recalls Turkey Bacon Products Due To Possible Adulteration

    Kraft Heinz is recalling approximately 2.1 million pounds of Oscar Mayer turkey bacon products that may spoil before their expiration dates.

    Product
    Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Turkey Bacon Products Due To Possible Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V539000·2015-08-24

    East Manufacturing Recalls 2014-2016 Trailers Due to Wheel Bearing Fire Risk

    East Manufacturing is recalling 2014-2016 trailers because insufficient grease in wheel hubs may cause overheating, leading to fire or wheel detachment.

    Product
    EAST MANUFACTURING — EAST MANUFACTURING FRAME GENESIS TRAILER, DUMP TRAILER, FRAMELESS GENESIS TRAILER, REFUSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V538000·2015-08-24

    McNeilus Recalls 2014-2015 CNG Trucks Due to Pressure Relief Defect

    McNeilus is recalling 2014-2015 CNG Refuse and Concrete trucks because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS CNG REFUSE TRUCK, CNG CONCRETE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V537000·2015-08-24

    BMW Recalls 2013-2015 G 650 GS Motorcycles for Stalling Risk

    BMW is recalling 1,060 G 650 GS and G 650 GS Sertao motorcycles because they may stall while idling with the clutch pulled in, increasing crash risk.

    Product
    BMW — BMW G 650 GS, G 650 GS SERATO
    Category
    Vehicle
    Distribution
    Distributed nationwide