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.

Which agencies issued them

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.

53851–53875 of 78407

  • SevereFDA (Food)·F-0420-2016·2016-01-13

    ConAgra Recalls David Trail Mix Sweet & Salty for Undeclared Milk

    ConAgra Foods is recalling David Trail Mix Sweet & Salty bags because they contain undeclared milk. The product was distributed nationwide and to specific foreign locations.

    Product
    David Trail Mix Sweet & Salty individual plastic bags net wt. 5 oz. (142 g) UPC 00 26200 23885 2 shipped in the following configurations: 1) cases of eight (8) with UPC 20-0-26200-23885-6; 2) 36-count multi-pack shipper case UPC 00-0-26200-23890-6 which contains 16…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0588-2016·2016-01-13

    Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recall for Handle Separation

    Boston Scientific is recalling ACUITY Pro Coronary Sinus Guide Catheters due to a potential for the proximal handle to separate from the shaft.

    Product
    Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr. Model 8104, 8105, 8106, 8107, 8108, 8109, 8110, 8111, 8112, 8113, 8114, 8115, 8116, 8117, 8118, and 8119. The ACUITY Pro Lead Delivery System is designed for venous use to aid in the selective placement of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0426-2016·2016-01-13

    Pine Valley Foods Recalls Sugar and Walnut Cookie Dough for Allergens

    Pine Valley Foods is recalling pre-portioned sugar and walnut chocolate chunk cookie dough because they contain undeclared milk and egg, respectively.

    Product
    Crazy about Cookies 2.7lb Sugar Cookies Pre-Portion Item # 25-2004 UPC Code - 698768102120
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0430-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Birthday Celebration COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4033 UPC Code - 698768034339
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0432-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookies for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie products due to undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb DSC Custom Decorated Sugar Cookies Item # 101-2207 thru 101- 2355 UPC Code - None
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0429-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Monster Bash COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4032 UPC Code - 698768034322
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0431-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific Hello Kitty sugar cookie kits because they contain undeclared milk and egg.

    Product
    Crazy about Cookies 2lb HELLO KITTY COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4035 UPC Code - 698768034353
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0592-2016·2016-01-13

    Biomet 3i Protection Cap Kits Recalled for Inadequate Biocompatibility Testing

    Biomet 3i is recalling 30,111 Protection Cap Kits worldwide due to inadequate biocompatibility testing. The devices are used as accessories for dental implants.

    Product
    BIOMET 3i, PROVIDE PROTECTION CAP KITS, Catalog # PAK4140, PAK4155, PAK4240, PAK4255, PAK4340, PAK4355, PAK4440, PAK4455, PAK5140, PAK5155, PAK5240, PAK5255, PAK5340, PAK5355, PAK5440, PAK5455, PAK6140, PAK6155, PAK6240, PAK6255, PAK6340, PAK6355, PAK6440, and PAK6455 BIOMET…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0574-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 1,406 post-operative knee braces because they may fail to maintain a locked position, potentially causing loss of balance or undesired knee movement.

    Product
    Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 10 units of the Brielle Ortho Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.

    Product
    BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0577-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 42 units of the Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.

    Product
    ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0605-2016·2016-01-13

    Baxter Y-Type Spike Adapter Recalled for Potential Particulate Matter

    Baxter Healthcare is recalling Y-Type Spike Adapters due to the potential presence of dark loose particulate matter on the spike.

    Product
    Baxter Y-Type Spike Adapter, 7" (18 cm), 1C8433, Product Usage: C8433: For the administration of fluids from a container into the patients vascular system through a vascular access device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2016·2016-01-13

    Made In Nature Recalls Sriracha Chili Kale Chips for Undeclared Soy

    Made In Nature is recalling Sriracha Chili Kale Chips due to undeclared soy allergen from Tamari. The recall covers 50,176 units distributed nationwide.

    Product
    Made In Nature Sriracha Chili Kale Chips, 2.2oz or 62g, In a clamshell container with a paper sleeve, 8 packages per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0593-2016·2016-01-13

    Biomet 3i Dental Impression Copings Recalled for Inadequate Biocompatibility Testing

    Biomet 3i is recalling specific dental impression copings due to inadequate biocompatibility testing. The devices are distributed worldwide, including in the US.

    Product
    BIOMET 3i, PROVIDE IMPRESSION COPINGS, Catalog # PIC484, PIC484H, PIC485, PIC485H, PIC654, PIC654H, PIC655, and PIC655H BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0572-2016·2016-01-13

    Partners In Medicine Recalls CNSystems Task Force Monitor 3040i for Blood Pressure Errors

    Partners In Medicine is recalling 28 CNSystems Task Force Monitor 3040i devices because they may provide incorrect blood pressure readings for some patients.

    Product
    CNSystems TASK FORCE MONITOR 3040i, plethysmograph, impedance. Noninvasively measure and display patient's hemodynamic parameters time synchronized using Impedance Cardiography (ICG), Electrocardiography (ECG), oscillometric Blood Pressure (oscBP) and continuous Blood Pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0594-2016·2016-01-13

    Biomet 3i Recall Dental Impression Coping Kits for Biocompatibility Testing

    Biomet 3i is recalling 30,111 Provide Impression Coping Kits worldwide due to inadequate biocompatibility testing.

    Product
    BIOMET 3i, PROVIDE IMPRESSION COPING KITS, Catalog # PRK484, PRK485, PRK654, and PRK655 BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V009000·2016-01-13

    Turtle Top Recalls Wheelchair Lifts Due to Bearing Failure Risk

    Turtle Top is recalling specific wheelchair lifts installed in Odyssey and Terra Transport vehicles because pivot holes may allow bearings to move, risking platform failure.

    Product
    TURTLE TOP — TURTLE TOP ODYSSEY XL, ODYSSEY LT, ODYSSEY, TERRA TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V008000·2016-01-13

    Newmar Recalls Motorhomes Due to Unstable Electric Entry Steps

    Newmar is recalling specific 2008-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    NEWMAR — NEWMAR BAY STAR, DUTCH STAR, VENTANA, CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V010000·2016-01-13

    Champion Bus Recalls 2009-2015 Models Due to Seat Belt Anchor Defect

    Champion Bus is recalling 2009-2015 Crusader, Stacked Rail, and CTS-RE vehicles because missing welds on seat brackets could cause seat belts to detach in a crash.

    Product
    CHAMPION — CHAMPION STACKED RAIL, CRUSADER, CTS-RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0589-2016·2016-01-13

    Maquet HCU 30 Heater-Cooler Unit Recalled for Power Supply Board Failure

    Maquet is recalling HCU 30 Heater-Cooler Units due to a power supply board defect that can cause overheating and unit shutdown during cardiopulmonary bypass procedures.

    Product
    Maquet HCU 30 Coolant Type R134A Filling weight 250 g 120 V 50-60 Hz 1920 W Product Usage: The Heater Cooler Unit (HCU) 30 is intended to circulate water through heat exchange circuits to warm or cool a patient during short duration cardiopulmonary bypass procedures lasting 6…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0335-2016·2016-01-13

    Made In Nature Recalls Sriracha Kale Chips Due to Undeclared Soy Allergen

    Made In Nature is recalling Sriracha Chili Kale Chips and Pacific Superfoods Snack Lava Rock Sriracha Kale Chips because they contain undeclared soy from Tamari.

    Product
    Pacific Superfoods Snack Lava Rock Sriracha Kale Chips, 2.2oz or 62g, In a clamshell container with a paper sleeve, 8 packages per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0580-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 80 post-operative knee braces that may fail to maintain the locked position, potentially causing loss of balance or undesired knee movement.

    Product
    CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0601-2016·2016-01-13

    3M Coban Self-Adherent Wrap Recalled for Latex Mislabeling

    3M is recalling Coban Self-Adherent Wrap mislabeled as latex-free because it actually contains latex, posing a risk to users with latex sensitivity.

    Product
    3M Coban Self-Adherent Wrap Shipper carton label identified the product as 3M Coban LF Latex Free Catalog #2081, lot number 2018-10AM.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0579-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling specific Post-Operative Knee Brace Lite models because they may fail to maintain the locked position, potentially causing loss of balance or undesired knee movement.

    Product
    ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0604-2016·2016-01-13

    Elekta Oncentra VMAT Radiation Therapy Planning System Recalled for Software Error

    Elekta, Inc. is recalling 154 units of the Oncentra External Beam - VMAT radiation therapy planning system because a software error may cause the system to incorrectly include organs at risk as target volumes.

    Product
    Oncentra External Beam - VMAT - Radiation therapy planning system Product Usage: The Oncentra system is a radiation treatment planning software designed to analyze and plan radiation treatments in three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide