The Recall Desk

State

Nebraska product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46601–46625 of 78389

  • CriticalFDA (Food)·F-1975-2017·2017-04-26

    Dutch Valley Holiday Delight Box Cheese Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Holiday Delight Boxes containing Guggisberg cheese products due to Listeria monocytogenes contamination.

    Product
    Holiday Delight Box Containing packages of Guggisberg Colby Cheese, Guggisberg Farmers Cheese & Guggisberg Marble Cheese.
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1968-2017·2017-04-26

    Guggisberg Farmers Cheese Recalled Due to Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Farmers Cheese because the supplier reported Listeria monocytogenes contamination.

    Product
    GUGGISBERG FARMERS CHEESE INGREDIENTS: Pasteurized Part Skim-Milk, Cultures, Salt, Enzymes, 1 lb, & 6 lb Distributed by: Guggisberg Cheese, 5060 S.R. 557, Milllersburg, OH 44654
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1974-2017·2017-04-26

    Holiday Cheese Baskets Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Holiday Crowd Pleaser Baskets containing Guggisberg Marble Cheese due to Listeria monocytogenes contamination.

    Product
    Holiday Crowd Pleaser Basket Containing packages Guggisberg Marble Cheese.
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1977-2017·2017-04-26

    Dutch Valley Recalls Amish Sampler Cheese Boxes Due to Listeria

    Dutch Valley Food Distributors is recalling Ultimate Amish Sampler Boxes containing Guggisberg cheeses due to Listeria monocytogenes contamination.

    Product
    Ultimate Amish SAmpler Box Containing packages of Guggisberg Colby Cheese, Guggisberg Marble Cheese.& Guggisberg Pepperjack Cheese.
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1972-2017·2017-04-26

    Guggisberg Christmas Baskets Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Country Christmas Baskets containing Biery Cheddar and Pepper Jack Cheese due to Listeria monocytogenes contamination.

    Product
    GUGGISBERG Country Christmas Basket Containing packages of Biery Cheddar and Pepper Jack Cheese 11275 W 250 MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1967-2017·2017-04-26

    Guggisberg Natural Cheese Marble Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Natural Cheese Marble because the supplier notified them that the product was contaminated with Listeria monocytogenes.

    Product
    GUGGISBERG NATURAL CHEESE MARBLE INGREDIENTS: Pasteurized Milk, Cultures, Enzymes, Salt, Annatto Color 1 lb, 2 lb, 6 lb & 15 lb 11275 W 250 N MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1991-2017·2017-04-26

    Dawn Food Products Recalls R&H Speedy Creme Vanilla Filling Mix

    Dawn Food Products Inc. is recalling R&H Speedy Creme Vanilla Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H Speedy Creme Vanilla Filling Mix Item 01148908 25 pound bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1821-2017·2017-04-26

    Philips UNIQ X-ray Systems Recalled for Potential Fire Hazard

    Philips is recalling UNIQ X-ray systems because a leak in the detector cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    UNIQ: UNIQ FD10 722026; UNIQ FD10/10 722027; UNIQ FD20/10 biplane 722029; UNIQ FD10 OR Table 722033; UNIQ FD10/10 OR Table 722034; UNIQ FD20/10 OR Table 722036; UNIQ FD20/20 722038; UNIQ FD20/20 biplane OR Table 722039
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1839-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number: 72204038 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1844-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: 72204043 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1843-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recalled for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: 72204042 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1838-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number: 72204037 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1990-2017·2017-04-26

    Dawn Food Products Recalls Vanilla Pudding Mix for Salmonella Risk

    Dawn Food Products is recalling R&H Vanilla Speedy Creme Instant Pudding and Pie Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mix Item 00727521 4 lbs 2 oz retail paper bag, six retail bags per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1842-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recalled for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills due to a potential for the cutting blade to detach or the drill head to fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: 72204041 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1973-2017·2017-04-26

    Guggisberg Cheese Gift Boxes Recalled Due to Listeria Contamination

    Dutch Valley Food Distributors is recalling 199 custom gift boxes of Guggisberg cheese products because they were contaminated with Listeria monocytogenes.

    Product
    Custom Gift Box Containing various packages of Guggisberg Cheese products
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Devices)·Z-1840-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: 72204039 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1820-2017·2017-04-26

    Philips Recalls Allura Xper Systems Due to Chiller Leak Fire Risk

    Philips is recalling specific Allura Xper medical imaging systems because a leak in the detector cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD10/10 722027; Allura Xper FD20/10 biplane 722029; Allura Xper FD10 OR Table 722033; Allura Xper FD10/10 OR Table 722034; Allura Xper FD20/10 OR Table 722036; Allure Xper FD20/20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1846-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: 72204045 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1851-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: 72204050 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1992-2017·2017-04-26

    Dawn Food Products Recalls Chocolate Pudding Mix for Salmonella Risk

    Dawn Food Products Inc. is recalling R&H Chocolate Speedy Creme Instant Pudding and Pie Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H CHOCOLATE Speedy Creme Instant Pudding and Pie Filling Mix Item 00257857 4 lbs 2 oz retail paper bag, six retail bags per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1971-2017·2017-04-26

    Guggisberg Cheese Lover's Box Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Cheese Lover's Boxes due to Listeria monocytogenes contamination reported by the supplier.

    Product
    GUGGISBERG Cheese Lover's Box Containing packages of Colby, Marble and Pepper Jack Cheese 11275 W 250 MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Devices)·Z-1841-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills due to a potential for the cutting blade to detach or the drill head to fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1822-2017·2017-04-26

    Philips Allura Xper Systems Recalled for Chiller Leak Fire Risk

    Philips is recalling specific Allura Xper systems equipped with Laird chillers because a leak in the cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 722003; Allura Xper FD10/10 722005; Allura Xper FD20 722006; Allura Xper FD20/10 and FD20/20 722008; Allura Xper FD10 722010…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V279000·2017-04-26

    Polaris Recalls 2016-2017 GEM Electric Vehicles for Loose Lug Nuts

    Polaris is recalling 2016-2017 GEM E2, E4, E6, and ELXD electric vehicles because front wheel lug nuts may loosen, potentially causing a wheel to detach.

    Product
    GEM — GEM E2, E6, E4, ELXD
    Category
    Vehicle
    Distribution
    Distributed nationwide