State

Kansas product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50001–50025 of 79646

HighFDA (Devices)·Z-0269-2017·2016-10-26
Windstone Medical Recalls Shoulder Arthroscopy Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,124 shoulder arthroscopy kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Shoulder Arthroscopy Pack, Kit number 002648-15, 002648-16, AMS2496, AMS2496(A, AMS2609, PSS2209(A, and PSS2209(B. convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0280-2017·2016-10-26
Windstone Medical Recalls Upper Extremity Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 108 Upper Extremity Packs because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Upper Extremity Pack, Kit number AMS2536 and AMS2536(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0248-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic is recalling disposable gloves used in custom surgical kits because splits or holes may compromise sterility.
Product
Nasal Pack, Kit number PSS2186 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2017·2016-10-26
Windstone Medical Recalls Hernia Packs With Defective Gloves
Windstone Medical Packaging is recalling 765 Hernia Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Hernia Pack, Kit number AMS1519 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0286-2017·2016-10-26
Windstone Medical Recalls Laparoscopy Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 50 laparoscopy kits because the disposable gloves included may contain splits or holes that compromise sterility.
Product
Laparoscopy Kit, Kit number PSS1038(A and PSS1038(B convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0177-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.
Product
Dr. Harrimans Kit, Kit number PSS3600 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0197-2017·2016-10-26
Windstone Medical Packaging Recalls General Surgery Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 985 general surgery kits because the Medtronic gloves included may have splits or holes that compromise sterility.
Product
General Plastics Pack, Kit number 008617-1 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0159-2017·2016-10-26
Windstone C-Section Kits Recalled Due to Potential Glove Splits or Holes
Windstone Medical Packaging is recalling C-Section kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
C-Section Pack, Kit number 002643-10, 002643-9, and AMS4449 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0198-2017·2016-10-26
Windstone Medical Recalls General Surgery Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 168 General Surgery Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
General Surgery Pack, Kit number PSS1380(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0224-2017·2016-10-26
Windstone Medical Recalls Lipo Pack Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 40 Lipo Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Lipo Pack, Kit number AMS4420 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0267-2017·2016-10-26
Windstone Medical Packaging Recalls Surgical Set Up Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 16 surgical Set Up Packs because they may contain defective gloves that compromise sterility.
Product
Set Up Pack, Kit number PSS3574(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0255-2017·2016-10-26
Windstone Medical Recalls Ortho Pack Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 92 Ortho Pack kits because they may contain defective gloves with splits or holes that compromise sterility.
Product
Ortho Pack, Kit number PSS3466 and PSS3466(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0284-2017·2016-10-26
Windstone Medical Packaging Recalls Virginia Custom Pack Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling Virginia Custom Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Virginia Custom Pack, Kit number RMS1744 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0167-2017·2016-10-26
Windstone Medical Custom Surgery Kits Recalled for Sterility Compromise
Windstone Medical Packaging recalled 56 custom surgery kits because the included Medtronic gloves may contain splits or holes, compromising sterility.
Product
Custom Tray, Kit numbers: PSS1836 and PSS1836(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0228-2017·2016-10-26
National Foods Packaging Recalls Low Sodium Chicken Base Due to Lead
National Foods Packaging Inc is recalling 2,000 pounds of Low Sodium Chicken Base because a spice ingredient contained elevated levels of lead.
Product
National Foods Packaging Low Sodium Chicken Base in 50 lb white poly-lined paper bags
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0227-2017·2016-10-26
National Foods Packaging Recalls Chicken Base Due to Lead Contamination
National Foods Packaging Inc is recalling 8,825 lb of Chicken Base because a spice ingredient contained elevated levels of lead. The product was distributed in Indiana, Texas, and Virginia.
Product
National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0133-2017·2016-10-26
ConMed CORE Suction Irrigation Handpiece Recalled for Packaging Seal Crease
ConMed is recalling CORE Suction Irrigation Handpieces because a crease in the packaging seal may create an open channel that compromises the product's sterility.
Product
CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or Dual Bags, Catalog Number CD8302 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0164-2017·2016-10-26
Entenmann's Little Bites Chocolate Chip Muffins Recalled for Plastic Presence
BIMBO Bakeries USA Inc. is recalling Entenmann's Little Bites Chocolate Chip Muffins due to the presence of plastic in the product.
Product
Entenmann's Little Bites Chocolate Chip Muffins; 10 Pouches; Net Wt. 1 lb. 0.5 OZ. ; Bimbo Bakeries USA, Inc.; PO #976, Horsham, PA 19044. Best By: October 8, 2016/3098; UPC: 7203002111; Entenmann's Little Bites Chocolate Chip Muffins; 20 Muffins, 5 Pouches; Net Wt. 8.25 OZ.…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0090-2017·2016-10-26
Ortho-Clinical VITROS Chemistry LAC Slides Recalled Due to NAC Interference
Ortho-Clinical Diagnostics is recalling VITROS Chemistry LAC Slides because N-Acetylcysteine (NAC) can interfere with the assay results.
Product
VITROS Chemistry Products LAC Slides, REF/Product Codes 843 3880 (300 slides per sales unit) and 815 0112 (90 slides per sales unit), Unique Device Identifier Nos. 10758750004911 and 10758750004454, Rx ONLY, IVD --- For in vitro diagnostic use only. VITROS Chemistry Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0167-2017·2016-10-26
Nature's One Organic PediaSmart Beverage Recalled for Incorrect Scoop Size
Nature's One is recalling Organic PediaSmart Dairy Vanilla beverage cans because they contain a scoop that provides only 60% of the intended nutrition.
Product
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360 G) can Contains: milk, soy & coconut UPC 7 16514 88101 0 Manufactured for: Natures One, 8754 Cotter Street, Lewis Center, OH 43035
Category
Food
Distribution
49 states
ModerateFDA (Devices)·Z-0129-2017·2016-10-26
ConMed Recalls CORE Suction Irrigation Handpieces Due to Packaging Seal Creases
ConMed is recalling CORE Suction Irrigation Handpieces because creases in the packaging seal may create open channels that compromise the product's sterility.
Product
CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution Bags, Catalog Number CD8185 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0123-2017·2016-10-26
Randox Lipase Test System Recalled for Carryover Interference
Randox Laboratories is recalling 18 units of Lipase test kits due to carryover interference when run near LDL or Triglycerides assays.
Product
Randox Lipase (Colorimetric) Product Usage: A lipase test system is a device intended to measure the activity of the enzyme lipase in serum and plasma. Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas such as acute pancreatitis and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0134-2017·2016-10-26
ConMed CORE Trumpet Handpiece Recalled for Packaging Seal Crease
ConMed is recalling CORE Trumpet Handpieces because a crease in the packaging seal may create an open channel that compromises the product's sterility.
Product
CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe , Catalog Number CD8400 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0111-2017·2016-10-26
Zimmer Biomet Recalls Vanguard Distal Femoral Augments Due to Labeling Error
Zimmer Biomet is recalling five Vanguard Distal Femoral Augments because the product inside the carton does not match the label. The mismatched size is easily identified during surgery.
Product
Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. Correction of varus, valgus, or posttraumatic deformity. …
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0132-2017·2016-10-26
ConMed CORE Suction Irrigation Handpiece Recalled for Packaging Seal Defect
ConMed is recalling CORE Suction Irrigation Handpieces because a crease in the packaging seal may compromise the product's sterility.
Product
CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags, Catalog Number CD8300 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide