The Recall Desk

State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47901–47925 of 78397

  • ModerateFDA (Devices)·Z-1016-2017·2017-01-18

    Hospira Recalls Minibore Extension Sets Due to Solvent Occlusion

    Hospira is voluntarily recalling one lot of Minibore Extension Sets due to a confirmed report of solvent occlusion that may prevent priming and delay therapy.

    Product
    Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0998-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens Medical Solutions is recalling Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Bio mCT-S(40) 3R->4R Upgrade, Material Number 10250743 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0973-2017·2017-01-18

    GE Healthcare Recalls OEC 9800 Imaging Systems Due to Power Cable Failures

    GE Healthcare is conducting a voluntary field action for OEC 9800 systems because the workstation power cable assembly can cause intermittent power cord failures.

    Product
    OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic…
    Category
    Medical Device
    Distribution
    50 states
  • ModerateUSDA FSIS·006-2017·2017-01-18

    Burgers Ozark Country Cured Recalls Mislabeled Turkey Products

    Burgers Ozark Country Cured is recalling approximately 1,905 pounds of fully cooked turkey products due to misbranding. The products contain undeclared sodium nitrite.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Burgers Ozark Country Cured Recalls Poultry Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0986-2017·2017-01-18

    Bard Access Systems Recalls SafeStep Huber Needle Sets Due to Labeling Errors

    Bard Access Systems is recalling SafeStep Huber Needle Sets because some units may have needle lengths or gauges that differ from the label.

    Product
    SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood sampling through…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0996-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 102 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(64)-4R, Material Number 10248672 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1000-2017·2017-01-18

    Siemens Biograph mCT 20 Excel PET/CT Scanner Recall for Laser Cover Windows

    Siemens is recalling 51 Biograph mCT 20 Excel scanners because laser cover windows may fall off.

    Product
    BIOGRAPH mCT 20 Excel, Material Number 10507786 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0955-2017·2017-01-18

    VOCO Futurabond M+ adhesive recalled for labeling mix-up

    Voco GmbH is recalling 50 units of VOCO Futurabond M+ adhesive due to a labeling error where the product was marked as Futurabond M+ Universal Adhesive.

    Product
    VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with methacrylate-based restorative, core build-up or luting materials. It can be applied with phosphoric acid etching (selective enamel etching or total-etch) of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0429-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0994-2017·2017-01-18

    Siemens Biograph mCT X-4R Laser Cover Window Recall

    Siemens is recalling 71 Biograph mCT X-4R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-4R, Material Number 10248670 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0983-2017·2017-01-18

    Bausch & Lomb Recalls Algerbrush-II Ophthalmic Surgical Instruments

    Bausch & Lomb is recalling Algerbrush-II surgical instruments because some units shipped with outdated operating instructions.

    Product
    Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0992-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens is recalling 41 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1019-2017·2017-01-18

    Acumed Recalls OPT Croutons Synthetic Bone Substitute Due to Sterilization Documentation Issues

    Acumed LLC is recalling 83 units of OPT Croutons synthetic bone substitute because documentation for the sterilization dose was inadequate. The product was distributed in ten US states and Puerto Rico.

    Product
    OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium phosphate. The tricalcium phosphate is a soluble calcium phosphate salt.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0997-2017·2017-01-18

    Siemens Biograph mCT X-3R Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 18 Biograph mCT X-3R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-3R, Material Number 10248673 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·007-2017·2017-01-18

    Willow Tree Poultry Farm Recalls Misbranded Chicken Salad Products

    Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm, Inc. Recalls Chicken Salad Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0424-2017·2017-01-18

    Pfizer Recalls Cytotec Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.

    Product
    CYTOTEC — CYTOTEC (MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V037000·2017-01-17

    Highland Ridge RV Recalls 2017 Fifth Wheels and Travel Trailers for Gas Leak Risk

    Highland Ridge RV is recalling 2017 Open Range, Mesa Ridge, and Roamer models because the outside range can be stored with the gas valve open, creating a fire or explosion hazard.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, OPEN RANGE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V034000·2017-01-13

    Renegade RV Recalls Motorhomes Due to Seat Belt Anchorage Defect

    REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.

    Product
    RENEGADE RV — RENEGADE RV SPECIALTY SPRINTER, VIENNA, VILLAGIO, CORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17728·2017-01-12

    Nantucket Distributing Recalls Pre-Lit Christmas Trees Due to Fire Hazard

    Nantucket Distributing is recalling pre-lit artificial Christmas trees because the fuse can overheat and blow, posing a fire hazard. No injuries have been reported.

    Product
    Pre-Lit Globe Light Christmas trees
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17726·2017-01-12

    BRP Recalls Side-by-Side Off-Road Vehicles Due to Roll-Away Hazard

    BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V033000·2017-01-12

    GM Recalls 2016-2017 Chevrolet Suburban HD for Incorrect Rearview Mirror

    General Motors is recalling 2016-2017 Chevrolet Suburban HD vehicles equipped with a convex right-hand outside mirror instead of a non-convex one, which may cause drivers to misjudge distance.

    Product
    CHEVROLET — CHEVROLET SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide