The Recall Desk

State

Kansas product recalls

73,817 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,053
Severe
1,486
Most recent
2026-11-04

Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47201–47225 of 79639

  • CriticalFDA (Food)·F-1970-2017·2017-04-26

    Guggisberg Natural Cheese Thunder Jack Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Natural Cheese Thunder Jack due to Listeria monocytogenes contamination. The product was distributed to 20 states.

    Product
    GUGGISBERG NATURAL CHEESE THUNDER JACK INGREDIENTS: Pasteurized Milk, Cultures, Red & Green Peppers, Salt, Enzymes, Annatto Color, 1 lb, & 6 lb 11275 W 250 MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1969-2017·2017-04-26

    Guggisberg Natural Cheese Pepper Jack Recalled for Listeria Contamination

    Dutch Valley Food Distributors is recalling Guggisberg Natural Cheese Pepper Jack due to Listeria monocytogenes contamination reported by the supplier.

    Product
    GUGGISBERG NATURAL CHEESE PEPPER JACK INGREDIENTS: Pasteurized Milk, Cultures, Red & Green Peppers, Salt, Enzymes, 1 lb, & 6 lb 11275 W 250 MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    21 states
  • 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
  • CriticalFDA (Food)·F-1984-2017·2017-04-26

    Nutiva Plant Protein Shake Recalled for Undeclared Peanut Allergen

    Nutiva is recalling Nuture Vitality Organic Plant Protein Superfood 30 Shake - Chocolate due to undeclared peanut allergen detected in testing.

    Product
    Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Chocolate; Product # PBP101 - 10-1.2 oz. (34g) packets ; Packet UPC/Caddy UPC: 6-92752-10713-9, 6-92752-10714-6; Master Case UPC: 6-92752-10715-3. Product # PBP105 - 21.6 oz. HDPE jar; Unit UPC…
    Category
    Food
    Distribution
    21 states
  • 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 (Food)·F-1983-2017·2017-04-26

    Nutiva Nuture Vitality Organic Plant Protein Shake Recalled for Peanut Allergen

    Nutiva is recalling Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla due to the presence of peanut allergen.

    Product
    Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets; Packet UPC/Caddy UPC: 6-92752-10716-0; 6-92752-10717-7; Master Case UPC: 6-92752-10718-4. Product # PBP205 - 21.6 oz. HDPE jar; Unit UPC…
    Category
    Food
    Distribution
    21 states
  • 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