The Recall Desk

State

Nebraska product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58551–58575 of 78413

  • ModerateFDA (Devices)·Z-1348-2015·2015-04-08

    Microtek Medical Recalls Sterile Laser Resistant Wands Due to Latex Packaging

    Microtek Medical Inc is recalling sterile laser resistant wands because the packaging contains latex but lacks the required warning label.

    Product
    LASER RESISTANT WAND - STERILE, 7/8" X 8" (2.22cm x 20.32cm), REF 24013, QTY 10 EA, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1754-2015·2015-04-08

    Health One Pharmaceuticals Recalls San Ye Qing Dietary Supplements

    Health One Pharmaceuticals is recalling Complex Tablet San Ye Qing dietary supplements due to significant violations of cGMP regulations.

    Product
    Complex Tablet San Ye Qing, 120 tablets, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1668-2015·2015-04-08

    Health One Pharmaceuticals Recalls In Act Xtract Dietary Supplements

    Health One Pharmaceuticals is recalling In Act Xtract dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    In Act Xtract
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1337-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmet Systems Due to Latex Packaging

    Microtek Medical is recalling 10 Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY, LUMBAR BELT AND MOTOR MODULE, REF 11110STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2015·2015-04-08

    Microtek Smoke Evacuation Tubing Set Recalled for Latex Packaging Labeling Error

    Microtek Medical Inc is recalling 303 Smoke Evacuation Tubing Sets because the packaging contains latex but lacks the required warning label.

    Product
    Smoke Evacuation Tubing Set for Coherent CPG Handpiece, 7/8" x 16' (2.22 cm x 487.88 cm), REF 24244, QTY 3/CS, NON STERILE NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1773-2015·2015-04-08

    Health One Pharmaceuticals Recalls Vigerect Dietary Supplements

    Health One Pharmaceuticals is recalling Vigerect dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Vigerect
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1347-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tube Sets Recalled for Latex Packaging

    Microtek Medical Inc is recalling sterile smoke evacuator tube sets because the packaging contains latex without the required warning label.

    Product
    (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor, Sterile, REF 24155, QTY 10/CS, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1648-2015·2015-04-08

    Health One Pharmaceuticals Recalls Yin Vive Dietary Supplement

    Health One Pharmaceuticals is recalling Yin Vive dietary supplements due to significant violations of cGMP regulations.

    Product
    Yin Vive, 80 Veggie Capsules, 400mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1375-2015·2015-04-08

    BD Biosciences Recalls CD123 PE Reagent Due to Antibody Contamination

    BD Biosciences is recalling one lot of CD123 PE reagent because it contains a low amount of CD4 antibody, which may result in unexpected staining patterns.

    Product
    CD123 (9F5) PE Catalog number 649453 Analyte Specific Reagent
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-1673-2015·2015-04-08

    Health One Pharmaceuticals Recalls Shrink & Clean Dietary Supplement

    Health One Pharmaceuticals is recalling Shrink & Clean dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Shrink & Clean, 60 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1361-2015·2015-04-08

    King Systems Double Swivel Connector Recalled for Mislabeling

    King Systems Corp. is recalling 900 units of Double Swivel Connectors mislabeled as having a suction port. The error may cause a short procedure delay but poses no risk to patients.

    Product
    Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or gas mask. The double swivel connector with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1343-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tubing Recalled for Unlabeled Latex Packaging

    Microtek Medical is recalling smoke evacuator tubing because the packaging contains latex but lacks the required warning label.

    Product
    TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1653-2015·2015-04-08

    Health One Recalls True Woman Dietary Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling True Woman dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    True Woman, 60 Vege Capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1679-2015·2015-04-08

    Health One Pharmaceuticals Recalls Griffonia Seed Extract 5-HTP Capsules

    Health One Pharmaceuticals is recalling Griffonia Seed Extract 5-HTP Capsules due to significant violations of cGMP regulations for dietary supplements.

    Product
    Griffonia Seed Extract 5-HTP Capsule, 60 capsules, 100mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1718-2015·2015-04-08

    Health One Pharmaceuticals Recalls Fish Oil 200 for cGMP Violations

    Health One Pharmaceuticals is recalling Fish Oil 200 dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Fish Oil 200
    Category
    Food
    Distribution
    Distributed nationwide