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.

33376–33400 of 79558

HighFDA (Devices)·Z-0528-2020·2019-12-04
Zimmer Biomet Recalls HA Pins and Hoffman/Colles Pins Due to Cleaning Issues
Zimmer Biomet is recalling HA Pins and Hoffman/Colles Pins because elevated bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA60-12040 HAA60-12060 HAA60-13030 HAA60-13040 HAA60-13050 HAA60-13060 HAA60-13070…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0523-2020·2019-12-04
Zimmer Biomet Recalls Hip Systems Due to Cleaning Issues
Zimmer Biomet is recalling various hip arthroplasty systems because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 11-162813 21-103202 21-103203 21-103204 21-103205 21-103206 21-103207 21-103208 21-103209 21-103210 21-103211 21-103212 21-103215 21-104109 21-104110 21-104111…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0522-2020·2019-12-04
Zimmer Biomet Recalls Hennessy Left Constrained Glenoid Shoulder Implants
Zimmer Biomet is recalling Hennessy Left Constrained Glenoid Humeral Shoulder Implants due to elevated bacterial endotoxin and residual debris caused by a cleaning issue.
Product
HENNESSY LEFT CONST GLENOID HA, Item No. PM555360 UDI (01)00880304819597(17)260425(10)664030 Product Usage: Constrained Shoulder.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0531-2020·2019-12-04
Zimmer Biomet Recalls Guide Wires Due to Bacterial Endotoxin and Debris
Zimmer Biomet is recalling 2.0mm Ball Nose Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
2.0MM BALL NOSE GUIDE WIRE, Item Nos. 281017006 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2020·2019-12-04
Zimmer Biomet Recalls Ball Nose Guide Wires Due to Cleaning Issues
Zimmer Biomet is recalling Ball Nose Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
BALL NOSE GUIDE WIRE 80CM, 100CM. Item Nos. 281001080 281001100 Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0580-2020·2019-12-04
Boston Scientific Recalls Rebel Monorail Coronary Stent Systems
Boston Scientific is recalling 14,145 Rebel Monorail PtCr Coronary Stent Systems because they may be missing a hydrophilic coating step.
Product
Rebel Monorail PtCr Coronary Stent System, REF / Catalog No. H7493927324300, Rebel MR OUS 3.0mm x 24mm. The Rebel Monorail (MR) Stent System is a balloon expandable Platinum Chromium (PtCr) Alloy stent pre-mounted on a Monorail Catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0583-2020·2019-12-04
GN Hearing Recalls Behind-the-Ear Hearing Aids Due to Software Bug
GN Hearing is recalling 590 behind-the-Ear hearing aids because a software bug in a repair tool altered sound amplification specifications, potentially increasing gain.
Product
Behind-the-Ear hearing aids, Model Numbers: Q962-DRW, T561-DRW, T562-DRW, T762-DRW, T777-DW, AMZ964-DRW, ET588-DWH, ET598-DW, ET788-DWH, ET798-DW, ET988-DWH, ET998-DW, FT861-DRW, FT862-DRW, RE561-DRWC, RE762-DRW, RE961-DRWC, RE962-DRW, PZ862-DRW, LT561-DRW, LT561-DRWZ…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0524-2020·2019-12-04
Zimmer Biomet Recalls HHR Tess Cleats Due to Bacterial Endotoxin
Zimmer Biomet is recalling Comprehensive HHR Tess Cleats because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
Comprehensive HHR Tess Cleat, Item Nos. 110260 110261 110262 110263 Product Usage: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0516-2020·2019-12-04
Beckman Coulter Recalls UniCel DxH Slidemaker Stainer Devices Due to Bent Probe Risk
Beckman Coulter is recalling UniCel DxH Slidemaker Stainer devices because a bent dispense probe may cause cell carryover, leading to erroneous lab results and potential inappropriate patient treatment.
Product
UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Stainer II (DxH SMS II) - Product Usage: The intended use is as follows: The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole-blood sample, smears a blood…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0575-2020·2019-12-04
Abbott Recalls Alinity c Carbon Dioxide Reagent Kits Due to CO2 Absorption
Abbott is recalling Alinity c Carbon Dioxide Reagent Kits because atmospheric carbon dioxide can be absorbed into the reagent, potentially causing incorrect test results.
Product
Alinity c Carbon Dioxide Reagent Kit, Produced for Abbott by Sekisui Diagnostics P.E.I. Inc. Prince Edward Island Canada
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V864000·2019-12-04
Ford Recalls 2017-2019 Super Duty Trucks for Tailgate Latch Defect
Ford is recalling 2017-2019 Super Duty trucks because water intrusion may cause the tailgate to open unexpectedly, creating a road hazard.
Product
FORD — FORD F-350 SD, F-250 SD, F-450 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0525-2020·2019-12-04
Zimmer Biomet Recalls Comprehensive RS Cleat CAP Due to Contamination
Zimmer Biomet is recalling Comprehensive RS Cleat CAP devices because elevated levels of bacterial endotoxin and residual debris remain on the products due to a cleaning issue.
Product
Comprehensive RS Cleat CAP, Item No. 110300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0527-2020·2019-12-04
Zimmer Biomet Recalls Copeland HA Resurfacing Heads Due to Cleaning Issues
Zimmer Biomet is recalling Copeland HA Resurfacing Heads because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0529-2020·2019-12-04
Zimmer Biomet Recalls Guide Wires Due to Bacterial Endotoxin and Debris
Zimmer Biomet is recalling specific Aim/Art Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
GUIDE WIRE 2.2MM X 28IN, Aim/Art Guide wire, Item No. 809222028 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0577-2020·2019-12-04
Boston Scientific Recalls Emerge Monorail PTCA Catheters Due to Coating Defect
Boston Scientific is recalling Emerge Monorail PTCA Dilatation Catheters because they may lack a required hydrophilic coating. The recall covers 14,145 devices distributed nationwide and in Canada.
Product
Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493919308200 EMERGE MR, OUS 2.00mm X 8mm; 2. REF/Catalog No. H7493918912200, EMERGE MR US 2.00MM X 12MM; 3. REF/Catalog No.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0518-2020·2019-12-04
Becton Dickinson Recalls Site~Rite 8 Ultrasound Systems Due to Battery Indicator Defect
Becton Dickinson is recalling 2,215 Site~Rite 8 Ultrasound Systems because the battery indicator may falsely show charge, causing abrupt shutdowns without warning.
Product
Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound System, Catalog No.9770500 Refurbished, Site~Rite¿ 8 System, Catalog No.9770500R Site~Rite 8 Ultrasound System, Catalog No.9770501 Refurbished Site~Rite¿ 8…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2020·2019-12-04
Zimmer Biomet Recalls Total Elbow Replacement Devices Due to Cleaning Issues
Zimmer Biomet is recalling specific total elbow replacement devices because elevated levels of bacterial endotoxin and residual debris remain on them due to a cleaning issue.
Product
LT DISC ULNA - HA/PC; RT DISC ULNA - HA/PC; LT DISC HMRL- HA/PC; RT DISC HMRL- HA/PC; DISC XS ULNA POR; DISC SEG ULNA POR; and Custom devices Item Nos. 114754 114755 114744 114745 114704 114705 114756 114757 114714 114715 114746 114747 114706 114707…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0534-2020·2019-12-04
Nextremity Solutions Recalls Stratum Foot Plating System Screws Due to Incorrect Specifications
Nextremity Solutions is recalling 49 units of Stratum Foot Plating System screws because they may contain the incorrect screw type and length.
Product
Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The Stratum Foot Plating System is a plate and screws construct indicated for fixation of fractures, osteotomies, nonunions, malunions and fusions of small bones and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0513-2020·2019-12-04
Medline Recalls EVENCARE G3 Blood Glucose Test Strips Due to Seal Defects
Medline Industries is recalling EVENCARE G3 Blood Glucose Test Strips because incomplete seals may cause the strips to expire prematurely.
Product
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2020·2019-12-04
Boston Scientific Recalls Advanix Pancreatic Stents Due to Shelf Life Labeling Error
Boston Scientific is recalling 54 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month duration.
Product
Advanix Pancreatic Stent, Straight Leading Barb, 10F x 6cm UPN: M00536640
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0545-2020·2019-12-04
Abbott Alinity ci Level Sensor Bulk Solution Recalled for Reliability Issues
Abbott is recalling Alinity ci Level Sensor Bulk Solution kits due to potential cracks caused by environmental stress, which may affect reliability.
Product
Accessory kit, Alinity c containing Alinity ci Level Sensor, Bulk Solution
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0560-2020·2019-12-04
Boston Scientific Pancreatic Stent Recalled for Incorrect Shelf Life Labeling
Boston Scientific is recalling 35 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 18cm UPN: M00536730
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0553-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 97 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month duration.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 8cm UPN: M00536660
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0550-2020·2019-12-04
Boston Scientific Pancreatic Stent Recall Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month period.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 5cm UPN: M00536630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0512-2020·2019-12-04
Rocket KCH Fetal Bladder Drainage Catheter Recalled for Kinking and Off-Label Use
Rocket Medical Plc is recalling 1,081 KCH Fetal Bladder Drainage Catheters due to reported kinking and off-label use for pleural drainage.
Product
Rocket KCH Fetal Bladder Drainage Catheter Model: R57405
Category
Medical Device
Distribution
Distributed nationwide