State

Kansas product recalls

73,737 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,821
Critical: 1,053
Severe: 1,485
Most recent: 2026-10-28

Of the 5,821 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 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32201–32225 of 79558

HighFDA (Devices)·Z-1303-2020·2020-02-26
Nobel Biocare Recalls Tapered Dental Drills Due to Sterility Concerns
Nobel Biocare is recalling 8 units of tapered dental drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Drill Tapered NP 3.5x8 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2020·2020-02-26
Siemens Recalls ADVIA Chemistry CardioPhase hsCRP Calibrator Due to Accuracy Drift
Siemens Healthcare Diagnostics is recalling 844 units of ADVIA Chemistry CardioPhase hsCRP Calibrator because accuracy has drifted from reference materials, causing high bias in quality control and patient sample recovery.
Product
ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP) Calibrator - product Usage: For in vitro diagnostic use in the calibration of ADVIA¿ Chemistry systems for the CardioPhase¿ hsCRP assay.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1232-2020·2020-02-26
Siemens Dimension Enzymatic Creatinine Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling Dimension Enzymatic Creatinine reagent because it may produce falsely low results for patients taking phenindione.
Product
Dimension Enzymatic Creatinine (EZCR) reagent, SMN 10471520
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0730-2020·2020-02-26
Safeway Cream Cheese Icing Recalled for Plastic Polymer Contamination
CSM Bakery Products is recalling 32 lb. pails of Safeway Cream Cheese Icing because pieces of plastic polymer were introduced into the sugar system.
Product
32 lb. pail SAFEWAY CREAM CHEESE ICING, MDM # 10203458, Distributed by Safeway Inc. PO Box 99 Pleasanton, CA 94566-0009
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0720-2020·2020-02-26
CSM Bakery Products Recalls Frozen Chocolate Chip Cookie Dough Due to Plastic
CSM Bakery Products is recalling specific lots of frozen chocolate chip cookie dough because pieces of plastic polymer were introduced into the sugar system.
Product
30 lb. cases of 480 1.0 oz frozen chocolate chip cookie dough, MDM # 10194622, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2020·2020-02-26
Philips CombiDiagnost GCF X-ray System Software Recall
Philips is recalling 116 CombiDiagnost GCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.
Product
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1231-2020·2020-02-26
Siemens Atellica CH Enzymatic Creatinine Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling Atellica CH Enzymatic Creatinine reagent due to potential falsely depressed results for patients on phenindione therapy.
Product
Atellica CH Enzymatic Creatinine (ECRE_2) reagent, SMN 11097533
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1339-2020·2020-02-26
Siemens Ysio Max Radiographic System Recalled for Software Bug
Siemens Medical Solutions is recalling 507 Ysio Max radiographic systems because a software bug may assign one image to two different patients, potentially affecting medical diagnosis.
Product
Ysio Max, model no. 10762470 - Product Usage: The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures f the whole body including: skull, chest, abdomen, and extremities and may be used on…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1275-2020·2020-02-26
Polysorb Suture Recall Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact sterility.
Product
Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11, Item Code CL537 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1280-2020·2020-02-26
Recall of Polysorb Braided Absorbable Suture Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24, Item Code CL911 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2020·2020-02-26
Nobel Biocare Recalls Tapered Drills Due to Sterility Concerns
Nobel Biocare is recalling 473 tapered dental drills because a packaging defect may compromise sterility during shelf life.
Product
Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2020·2020-02-26
FDA Recalls Polysorb Suture Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that could impact sterility.
Product
Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10, Item Code SL1625G - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2020·2020-02-26
Nobel Biocare Guided Tapered Drills Recalled for Sterility Concerns
Nobel Biocare is recalling 346 Guided Tapered Drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise sterility.
Product
Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21, Item Code CL811 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2020·2020-02-26
Nobel Biocare Recalls Screw Taps Due to Packaging Seal Defects
Nobel Biocare is recalling Screw Tap Tapered WP Single-Pat devices because a packaging sealing defect may compromise sterility during shelf life.
Product
Screw Tap Tapered WP Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2020·2020-02-26
Siemens Luminos dRF Max Recalled for Collision Control Override Risk
Siemens is recalling 46 Luminos dRF Max devices because an override function can disable collision controls, creating a risk of collision with obstacles or persons.
Product
Luminos dRF Max, Model No. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1310-2020·2020-02-26
Nobel Biocare Tapered Drills Recalled Due to Sterility Concerns
Nobel Biocare is recalling 154 units of Tapered RP 4.3x13 mm drills because a packaging defect may compromise sterility.
Product
Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 0 30" VIOLET GU-46, Item Code UL877 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1318-2020·2020-02-26
Nobel Biocare Implant Retrieval Instrument Recall Due to Sterility Concerns
Nobel Biocare is recalling 31 units of Implant Retrieval Instrument CC 3.0 31 mm because a packaging sealing defect may compromise sterility.
Product
Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0728-2020·2020-02-26
CSM Bakery Products Recalls Vanilla Buttercreme Frosting Due to Plastic Contamination
CSM Bakery Products is recalling 35 lb. pails of Vanilla Xtra Smooth Buttercreme Frosting because pieces of plastic polymer were introduced into the sugar system.
Product
35 lb. pail VANILLA XTRA SMOOTH BUTTERCREME FROSTING, MDM # 10203023, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2020·2020-02-26
Nobel Biocare Abutment Screw Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 233 units of Abutment Screw Retrieval Instruments because a packaging defect may compromise sterility during shelf life.
Product
Abutment Screw Retrieval Instrument 3.0/NP - Product Usage: The instruments for abutment screw retrieval can be used if an abutment screw is broken and a part of the screw is left inside the implant screw channel. If the implant thread needs to be cleaned before placing a new…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2020·2020-02-26
Smith & Nephew Recalls TwinFix Ti Suture Anchors Due to Sterility Risk
Smith & Nephew is recalling TwinFix Ti 2.8 mm HS Suture Anchors because a protective tube failure may have breached the sterile barrier.
Product
TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure attachment of soft tissue to bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1340-2020·2020-02-26
Siemens ARTIS Pheno-Interventional Fluoroscopic X-Ray System Recalled for Robotic Stand Defect
Siemens Medical Solutions is recalling 96 ARTIS Pheno-Interventional Fluoroscopic X-Ray Systems because safety brakes may block the robotic stand, preventing intended movements.
Product
ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 - Product Usage:AXIOM Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1306-2020·2020-02-26
Nobel Biocare Tapered Drills Recalled Due to Sterility Concerns
Nobel Biocare is recalling specific tapered dental drills because a packaging defect may compromise their sterility during shelf life.
Product
Drill Tapered NP 3.5x10 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0721-2020·2020-02-26
CSM Bakery Recalls Frozen Cookie Dough Due to Plastic Contamination
CSM Bakery Products is recalling frozen chocolate chip cookie dough because pieces of plastic polymer were introduced into the sugar system.
Product
30 lb. cases of 480 1.0 oz frozen chocolate chip with mini colored candy pieces cookie dough, MDM # 10194626, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide