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.

50676–50700 of 78397

  • SevereFDA (Food)·F-1771-2016·2016-08-03

    CRF Frozen Foods Recalls Mixed Vegetables Due to Listeria Risk

    CRF Frozen Foods is recalling specific lots of frozen mixed vegetables because they may be contaminated with Listeria monocytogenes.

    Product
    Mix Vegetables, brand JFDA (label in Japanese), frozen, net wt. 1 kg., UPC 991438945321 Mixed Vegetables, brand Mountain Mist, frozen, net wt. 1 kg., UPC 4635800055 The ingredients statement declares: Carrots, Corn, and Peas.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16764·2016-08-03

    National Time Fire Alarm Pull Stations Recalled for Handle Failure

    Signal Communications is recalling National Time fire alarm pull stations because the pull handle can break and fail to activate the alarm system.

    Product
    Fire alarm pull stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1829-2106·2016-08-03

    Frito-Lay Recalls Baked & Popped Mix for Potential Undeclared Peanuts

    Frito-Lay is recalling 20-count Baked & Popped Mix packages nationwide due to a potential undeclared peanut allergen.

    Product
    20 count Baked & Popped Mix packaged as 20 single flexible plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2293-2016·2016-08-03

    Elekta Recalls MOSAIQ Oncology System Due to Potential Dosing Errors

    Elekta is recalling 383 units of the MOSAIQ Oncology Information System because a software issue may prevent order changes from saving, potentially resulting in incorrect chemotherapy doses.

    Product
    MOSAIQ Oncology Information System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1831-2016·2016-08-03

    Frito-Lay Recalls Fun Times Mix for Potential Undeclared Peanuts

    Frito-Lay is recalling 32-count Fun Times mix packages nationwide due to a potential undeclared peanut ingredient.

    Product
    32 count Fun Times mix packaged as 32 single flexible plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1846-2016·2016-08-03

    Armour Snackmaker Keebler Animals Crackers Recalled for Peanut Residue

    Armour Eckrich Meats LLC is recalling Armour Snackmaker Keebler Animals Crackers due to potential low levels of peanut residue from a supplier ingredient.

    Product
    Armour Snackmaker Keebler Animals Crackers, Chocolate Icing with Natural and Artificial Flavors, Plain Icing which are packaged in 2.7oz packages; Unit UPC code 2781500240 . There are 18 packages to a case, Case SKU 2781500240. The responsible firm name on the label is…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2273-2016·2016-08-03

    Ortho-Clinical VITROS Calcium Slides Recalled for Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Calcium Slides due to potential negatively biased results that may affect diagnosis.

    Product
    VITROS Chemistry Products Ca Slides, GEN 29, REF/Product Code 145 0261, Unique Device Identifier No. 10758750009114 or 20758750009111, IVD -- Sales Unit: 300 slides/pack Product Usage: For in vitro diagnostic use only. VITROS Ca Slides quantitatively measure calcium (Ca)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1833-2016·2016-08-03

    Frito-Lay Recalls Home Town Favorite Variety Pack for Undeclared Peanuts

    Frito-Lay is recalling 30-count Home Town Favorite Variety Packs due to a potential undeclared peanut allergen. Consumers should check their 'guaranteed fresh' dates and manufacturing codes.

    Product
    30 count Home Town Favorite Variety Pack packaged as 30 single flexible plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V579000·2016-08-03

    Forest River Cherokee Recalled for Insufficient Tire Clearance

    Forest River is recalling 2017 Cherokee recreational trailers because insufficient clearance may damage tires, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2300-2016·2016-08-03

    Ge Healthcare Recalls Imagecast PACS Software Due to Image Context Defect

    Ge Healthcare is recalling Imagecast PACS software versions prior to 10.6 Update Package 18 because a defect causes images to be out of context with clinical information.

    Product
    Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 18 Product Usage: is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians. The system is used with general…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1830-2016·2016-08-03

    Frito-Lay Recalls SunChips and Rold Gold Mix for Undeclared Peanuts

    Frito-Lay is recalling 20-count SunChips & Rold Gold Mix packages due to a potential for undeclared peanuts. Consumers should stop eating the product and return it to the store.

    Product
    20 count SunChips & Rold Gold Mix packaged as 20 single flexible plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V577000·2016-08-03

    Toyota Recalls 4Runners for Exhaust Tip Burn Hazard

    Toyota is recalling 2010-2015 4Runners with aftermarket exhaust tips that may burn people standing behind the vehicle.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1827-2016·2016-08-03

    Rold Gold Pretzels Recalled for Potential Undeclared Peanuts

    Frito-Lay is recalling specific Rold Gold pretzel products due to the potential presence of undeclared peanuts.

    Product
    Rold Gold Tiny Twists 1 oz., 2 oz., 16 oz., and 20 1/2 oz.; Rold Gold Original Pretzel Thins 4 oz. and 16 oz.; Rold Gold Sticks 16 oz. packaged in flexible plastic bags.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16238·2016-08-03

    Porta Recalls Residential Elevators with Plastic Door Locks

    Porta Inc. is recalling about 60,000 residential elevators because plastic door locks may fail, allowing doors to open before the car arrives and posing a fall hazard.

    Product
    Residential elevators with electro mechanical door locks (EMDLs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1832-2016·2016-08-03

    Frito-Lay Recalls Baked and Popped Variety Pack for Undeclared Peanuts

    Frito-Lay is recalling 217,248 units of Baked and Popped Variety Packs nationwide due to potential undeclared peanuts.

    Product
    30 count Baked and Popped Variety Pack packaged as 30 single flexible plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2016·2016-08-03

    Zimmer Avenir Moller Hip Stem Recall Due to Packaging Mix-up

    Zimmer GmbH is recalling two Avenir Moller hip stem models due to a packaging mix-up that could lead to the use of the incorrect implant.

    Product
    Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis Intended Use: " Advanced wear of the joint due to degenerative, post-traumatic or rheumatic diseases. " Failed previous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2274-2016·2016-08-03

    Beckman Coulter Allegra X-5 Rotor Yoke Recalled for Defect

    Beckman Coulter is recalling Allegra X-5 rotor yokes because a defect allows improper rotor seating, which could lead to rotor failure if buckets are loaded in an imbalanced configuration.

    Product
    Allegra X-5 rotor yoke, Catalog No. (Instruments) B30589 and B30590 (Rotor) B30593. Product Labeling: IFU B29071AA. Product Usage: For In Vitro Diagnostic Use. The Allegra X-5 is intended for the separation of components through the use of relative centrifugal force. It is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2295-2016·2016-08-03

    Draeger Babytherm Infant Warmers Recalled for Skin Temperature Mode Risk

    Draeger Medical is recalling 1,599 Babytherm infant warmers due to a risk associated with operating the device in skin temperature mode without a patient connected.

    Product
    Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404 (Babytherm 8004), non sterile, software controlled. Product Usage: Babytherm 8004/8010 is an open care infant warmer system for warming premature babies, neonates…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2283-2016·2016-08-03

    LeMaitre Vascular Recalls Anastoclip AC Clips Due to Mislabeling

    LeMaitre Vascular is recalling 256 units of Anastoclip AC Clips because marketing materials incorrectly stated they could be used for dura closure.

    Product
    Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # 4000-06 The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is intended to remove Anastoclip AC Clips as necessary. It is an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1450-2016·2016-08-03

    Sagent Pharmaceuticals Recalls Oxacillin for Injection Due to Particulate Matter

    Sagent Pharmaceuticals is recalling Oxacillin for Injection due to the presence of small, dark particulate matter in the solution after reconstitution.

    Product
    Oxacillin for Injection, USP, 10 grams per pharmacy bulk package, Buffered - For IV Use, Sterile, Nonpyrogenic, Preservative-free, Rx Only, Mfd for Sagent Pharmaceuticals, Schaumberg, IL, 60196, USA, Made in India, NDC 25021-163-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2279-2016·2016-08-03

    Pentax Medical Video Processor Recalled for Uncleared Water Bottle Assembly

    Pentax Medical is recalling Video Processor EPK-i5010 units because they were shipped with a water bottle assembly not cleared for use in the United States.

    Product
    Ultrasound Gastroscope Product Usage: Intended to provide optical visualization of, ultrasonic Visualization of, and therapeutic access to the Upper Gastrointestinal Tract including but not restricted to, the organs; tissues; and subsystems: Esophagus, Stomach, Duodenum…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2287-2016·2016-08-03

    LeMaitre Vascular Recalls Anastoclip Universal Clip Remover for Mislabeling

    LeMaitre Vascular is recalling 39 units of the Anastoclip Universal Clip Remover because marketing materials incorrectly stated the device could be used for dura closure.

    Product
    AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is intended to remove Anastoclip AC Clips as necessary. It is an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2297-2016·2016-08-03

    Smith & Nephew Recalls Spherical Head Reflection Cancellous Screws Due to Labeling Error

    Smith & Nephew is recalling 185 units of Spherical Head Reflection 6.5 mm Cancellous Screws because the packaging contained 35mm screws instead of the labeled 25mm size.

    Product
    SPHERICAL HEAD REFLECTION(R) 6.5 MM CANCELLOUS SCREW, REF 71332525, QTY: (1), STERILE R, smith&nephew Total hip components are indicated for individuals undergoing primary or revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide