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.

47076–47100 of 79639

ModerateFDA (Devices)·Z-1895-2017·2017-05-10
Richard-Allan Scientific Recalls Shandon Rapid Chrome Kwik-Diff Kits
Richard-Allan Scientific is recalling Shandon Rapid Chrome Kwik-Diff Kits because the Methylene Blue Solution #3 was mislabeled and actually contained Crystal Violet.
Product
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707 Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990700 is sold as a kit in 500ml bottles. Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990707 is sold as…
Category
Medical Device
Distribution
24 states
ModerateFDA (Devices)·Z-1992-2017·2017-05-10
Anspach Compact Speed Reducer Recalled for Missing Service Interval Instructions
The Anspach Effort, Inc. is recalling 714 Compact Speed Reducers because the supplied directions for use did not contain a recommended service interval.
Product
Compact Speed Reducer, 60:1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2007-2017·2017-05-10
Anspach Effort Bearing Sleeve Recalled for Missing Service Interval Instructions
The Anspach Effort, Inc. is recalling 121 Bearing Sleeves because the supplied directions for use did not contain a recommended service interval.
Product
Bearing Sleeve, 15CM Straight Taper Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1910-2017·2017-05-10
Smith & Nephew Recalls Radial Osteotome Blades Due to Shelf Life Data
Smith & Nephew is recalling 1,416 units of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 12, REF 71369312, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1918-2017·2017-05-10
Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Shelf Life Data
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369410, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1972-2017·2017-05-10
Anspach Effort Recalls 11CM Angle Attachment for Missing Service Interval
The Anspach Effort, Inc. is recalling 45 units of the 11CM Angle Attachment, Black Max because the supplied directions for use did not contain a recommended service interval.
Product
11CM ANGLE ATTACHMENT, BLACK MAX
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1984-2017·2017-05-10
Anspach Effort 8.2cm Pneumatic Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 80 units of the 8.2cm Black Max pneumatic attachment because the supplied directions for use did not include a recommended service interval.
Product
8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2023-2017·2017-05-10
Anspach Effort Recalls 14cm QD Angle Attachments Due to Missing Service Interval
The Anspach Effort, Inc. is recalling 91 units of the 14cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.
Product
14cm QD Angle Attachment
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1913-2017·2017-05-10
Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Shelf Life
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 3 INCH, REF 71369208, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1944-2017·2017-05-10
Anspach Effort Recalls XMAX Pneumatic Drill System for Missing Service Interval
The Anspach Effort, Inc. is recalling 554 XMAX Pneumatic Drill Systems because the supplied directions for use did not include a recommended service interval.
Product
XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1920-2017·2017-05-10
Smith & Nephew Recalls Renovation Osteotome Blades Due to Shelf Life Data
Smith & Nephew is recalling Renovation osteotome blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 20 MM, REF 71369420, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1963-2017·2017-05-10
Anspach Effort Recalls Green Rotating Craniotomes for Missing Service Interval
The Anspach Effort, Inc. is recalling eight Green Rotating Craniotomes because the supplied directions for use did not contain a recommended service interval.
Product
GREEN ROTATING CRANIOTOME, BLACK MAX
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0688-2017·2017-05-10
Harvard Drug Group Recalls Fluconazole Tablets for Failed Dissolution
The Harvard Drug Group is recalling 2,341 cartons of Fluconazole 100 mg tablets because they failed to meet dissolution specifications.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2178-2017·2017-05-10
Source Naturals Vitamin D-3 Recalled for Lower Concentrations
Threshold Enterprises Ltd is recalling specific lots of Source Naturals Vitamin D-3 dietary supplements because testing found lower concentrations than labeled.
Product
Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% DV. Other ingredients: Vegetable Glycerin, Deionized water, citric acid, Natural orange flavor and lemon essential oil. Use 5 drops once daily in a drink.…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1954-2017·2017-05-10
Anspach Effort SC2100 Foot Control Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 22 SC2100 foot controls because the supplied directions for use did not contain a recommended service interval.
Product
Foot Control without Switches, SC2100 Product Usage: Electric system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2008-2017·2017-05-10
Anspach Effort Bearing Sleeve Recall for Missing Service Interval
The Anspach Effort, Inc. is recalling 58 Bearing Sleeve units because the supplied directions for use did not contain a recommended service interval.
Product
Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1912-2017·2017-05-10
Smith & Nephew Recalls Radial Osteotome Blades Due to Stability Data
Smith & Nephew is recalling specific lots of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0696-2017·2017-05-10
Akorn Recalls Sulfamethoxazole and Trimethoprim Oral Suspension for Dissolution Failures
Akorn Inc is recalling 55,968 bottles of Sulfamethoxazole and Trimethoprim Oral Suspension because the product failed to meet dissolution specifications.
Product
Sulfamethoxazole and Trimethoprim Oral Suspension, USP 200 mg / 40 mg per 5 mL , Grape Flavor, Rx Only, 16 fl oz. (473 mL), HI-TECH PHARMACAL CO., INIC, Amityville, NY 11701, NDC 50383-824-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2005-2017·2017-05-10
Anspach Effort Recalls Bearing Sleeves Due to Missing Service Interval Instructions
The Anspach Effort, Inc. is recalling 224 Bearing Sleeves because the supplied directions for use did not contain a recommended service interval.
Product
Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1957-2017·2017-05-10
Anspach Effort Recalls System Consoles Due to Missing Service Interval Instructions
The Anspach Effort, Inc. is recalling 239 System Console units because the supplied directions for use did not contain a recommended service interval.
Product
System Console, Single Port, no irrigation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2000-2017·2017-05-10
Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 10.5cm Long Attachments for pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1940-2017·2017-05-10
Anspach Effort Recalls 19cm Pneumatic Attachment Due to Missing Service Interval
The Anspach Effort, Inc. is recalling 41 units of the 19cm Attachment, Black Max, because the supplied directions for use did not include a recommended service interval.
Product
19cm Attachment, Black Max Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1958-2017·2017-05-10
Anspach Effort 7.2cm Adjustable Drill Guide Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 198 units of the 7.2cm Adjustable Drill Guide because the supplied directions for use did not contain a recommended service interval.
Product
7.2cm Adjustable Drill Guide Product Usage: Electric system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2010-2017·2017-05-10
Anspach Effort Recalls Minimal Access Attachments for Missing Service Interval
The Anspach Effort, Inc. is recalling 22 Minimal Access Attachments because the supplied directions for use did not contain a recommended service interval.
Product
Minimal Access Attachment, BLACK MAX Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1905-2017·2017-05-10
Breg Inc Recalls Sterile Dressings Due to Potential Unsealed Pouches
Breg Inc is recalling approximately 2,609 sterile dressings because a small percentage may have unsealed pouches, rendering them non-sterile.
Product
Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied…
Category
Medical Device
Distribution
Distributed nationwide