The Recall Desk

State

Nebraska product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32126–32150 of 78302

  • HighNHTSA·20V081000·2020-02-13

    Jaguar Recalls 2010 XF Vehicles Due to Fuel Leak Fire Risk

    Jaguar is recalling 2010 XF vehicles with 4.2L engines because a cracked fuel tank outlet flange may leak fuel, increasing fire risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V083000·2020-02-13

    BMW Recalls 2019 C 400 X Scooters for Throttle Cable Defect

    BMW is recalling 2019 C 400 X scooters because water in the throttle cable can freeze, causing the throttle to stick and increasing crash risk.

    Product
    BMW — BMW C 400 X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20073·2020-02-13

    Textron Recalls Gas-Powered Off-Road Vehicles Due to Fire Hazard

    Textron Specialized Vehicles is recalling approximately 20,573 gas-powered E-Z-GO, Cushman, and Tracker off-road vehicles because a starter generator wire can contact the exhaust, posing a fire hazard.

    Product
    Gas-powered E-Z-GO, Cushman and Tracker brand off-road vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0980-2020·2020-02-12

    Pacific Medical Fetal Transducers Recalled for Lack of Regulatory Clearance

    Pacific Medical Group Inc. is recalling 628 fetal transducers distributed without 510(k) clearance. The devices may fail to monitor vital signs, posing risks of burns or delayed detection of distress.

    Product
    Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX), FFCM3260
    Category
    Medical Device
    Distribution
    45 states
  • SevereFDA (Devices)·Z-1002-2020·2020-02-12

    Cardinal Health Recalls AAMI 3 Fabric Reinforced Gowns Due to Contamination

    Cardinal Health is recalling AAMI 3 Fabric Reinforced Gowns due to unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABRIC REINFORCEDGown 2XL NS, Item Code 9571NA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1014-2020·2020-02-12

    Cardinal Health Recalls RoyalSilk Gowns Due to Unknown Contamination

    Cardinal Health is recalling RoyalSilk gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    ROYALSILK 3XLARGE/XLONG NS, Gown Item Code 95998N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V079000·2020-02-12

    2019 Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Exhaust Leak

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vehicles because an exhaust gas leak could increase the risk of a fire.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 4500, SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0927-2020·2020-02-12

    Intuitive Surgical Recalls da Vinci SP Systems Due to Defective Capacitors

    Intuitive Surgical is recalling four da Vinci SP Surgical Systems because defective capacitors on circuit boards may cause vision loss or non-recoverable system errors.

    Product
    da Vinci SP Surgical System, SP1098, 00886874114605 Product Usage: used with an endoscope, surgical instruments, and accessories to perform minimally invasive surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1013-2020·2020-02-12

    Cardinal Health Recalls AAMI 3 Royalsilk Surgical Gowns Due to Contamination

    Cardinal Health is recalling AAMI 3 Royalsilk Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 ROYALSILK SURGGOWN BNS 2XL, Item Code 9578NB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1030-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns (4XL) because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 NONREINF SURGICAL GOWN 4XL, Item Code 9599
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1004-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABREINF SURG GOWN L NS, Item Code 9511NB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V075000·2020-02-12

    Forest River Recalls 2019-2020 Trailers Due to Spare Tire Carrier Defect

    Forest River is recalling 2019-2020 trailers because spare tire carrier U-bolts may fail, allowing the tire to detach and create a road hazard.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN INDEPENDENCE, R-POD, VIKING, PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1022-2020·2020-02-12

    Cardinal Health Recalls Royalsilk Gowns Due to Unknown Contamination

    Cardinal Health is recalling approximately 7.7 million Royalsilk gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    ROYALSILK LARGE, Gown. Item Code 9518
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1024-2020·2020-02-12

    Cardinal Health Recalls RoyalSilk Gowns Due to Unknown Contamination

    Cardinal Health is recalling RoyalSilk gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    ROYALSILK 3XLARGE/XLONG, Gown. Item Code 95998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2020·2020-02-12

    Intuitive Surgical Recalls da Vinci Systems Due to Defective Capacitors

    Intuitive Surgical is recalling 52 da Vinci X surgical systems worldwide due to defective capacitors that may cause vision loss or system errors.

    Product
    da Vinci X Surgical System Surgical System, IS4200, 00886874114216 Product Usage: used with an endoscope, surgical instruments, and accessories to perform minimally invasive surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V076000·2020-02-12

    Audi TT Recall: Fuel Tank Heat Shield Bracket Fire Risk

    Volkswagen is recalling 2016-2019 Audi TT vehicles because a fuel tank heat shield bracket may damage the tank in a crash, causing a fuel leak and fire risk.

    Product
    AUDI — AUDI TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0976-2020·2020-02-12

    Cook Inc. Recalls Sof-Flex Ureteral Stent Sets Due to Loading Error

    Cook Inc. is recalling 13,388 Sof-Flex Multi-Length Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient.

    Product
    Sof-Flex Multi-Lenqth Ureteral Stent Set, Global Product No. G14773 G15000 G14867 G14951 G17852
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1008-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels

    Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABRNF SCRUB SURG GWN XL NS, Gown. Item Code 91070NB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V078000·2020-02-12

    2019 Mercedes-Benz and Freightliner Sprinter EGR Pipe Fire Risk Recall

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because loose EGR pipe screws may allow hot exhaust gases to leak, increasing the risk of a fire.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1016-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 non-reinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 NONREIN SCRBNURGOWN BNS L, Item Code 90270NB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1099-2020·2020-02-12

    Stryker Telescopic Bovie Pencil Recalled for Electrical Arcing Risk

    Stryker is recalling 15,150 telescopic Bovie pencils due to hairline fractures that could cause electrical arcing and burns.

    Product
    Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1023-2020·2020-02-12

    Cardinal Health Recalls ROYALSILK Gowns Due to Unknown Contamination

    Cardinal Health is recalling ROYALSILK gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    ROYALSILK 2XLARGE, Gown. Item Code 9578
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1011-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels

    Cardinal Health is recalling AAMI 3 Royalsilk Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 ROYALSILK SURGGOWN BNS L, Gown. Item Code 9518NC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1040-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABREINF SURG GOWN LARGE, Item Code 9511
    Category
    Medical Device
    Distribution
    Distributed nationwide