State

Kansas product recalls

72,971 recalls have nationwide distribution and so reach Kansas. 5,725 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,725
Critical: 1,046
Severe: 1,228
Most recent: 2026-09-16

Of the 5,725 recalls naming Kansas we have scored against our rubric, 1,046 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,725 recalls whose distribution notice names Kansas specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5626–5650 of 78696

ModerateFDA (Devices)·Z-2417-2025·2025-09-03
NovoTHOR XL devices recalled over failed welded nut detaching gas strut
NovoTHOR XL devices, model S2190, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 55 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2422-2025·2025-09-03
Atlantis IO FLO-S kits recalled over thread defect limiting implant engagement
Atlantis IO FLO-S Kits, catalog A04S / 68020034, are recalled because a thread defect stops the device fully engaging an implant or analog, engaging about two rotations instead of five. 780 units are affected.
Product
Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04S / 6802034 Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure with the aim of restoring che
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2475-2025·2025-09-03
Anti-Xa test kits recalled over potential contamination by fibrinogen reagents
STA-Liquid Anti-Xa 8 kits are recalled because of the potential for contamination by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 126,200 units are affected.
Product
STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparin
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2474-2025·2025-09-03
Anti-Xa 4 test kits recalled over potential fibrinogen reagent contamination
STA-Liquid Anti-Xa 4 kits are recalled because of the potential for contamination by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 116,600 units are affected.
Product
STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparins
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0596-2025·2025-09-03
Acetaminophen injection containers recalled after discoloration found in one lot
Baxter Acetaminophen Injection 1000 mg/100 mL in Viaflo containers, lot 24A27G66, is recalled nationwide because of discoloration. 13,000 containers are affected.
Product
ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2477-2025·2025-09-03
Medication dispensing stations recalled because antivirus software was not consistently installed
BD Pyxis MedStation and Anesthesia Station devices are recalled because antivirus software was not consistently installed during implementation. 8,353 devices are affected, 6,738 of them in the US.
Product
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis" MedStation" ES Tower / 10885403512674 / 352 BD Pyxis" Anesthesia Station ES / 10885403477836 / 327 BD Pyxis" MedStation" ES (Main) / 10885403512667 / 323
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2421-2025·2025-09-03
Dental implant locating kits recalled over thread defect limiting full engagement
Atlantis IO FLO-S Kits are recalled because a thread defect stops the device fully engaging an implant or analog, engaging about two rotations instead of five. 102 units are affected.
Product
Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure wit
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2398-2025·2025-09-03
S8-3t ultrasound probes recalled for labelling defining device useful life
S8-3t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S8-3t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2388-2025·2025-09-03
OMNI III TEE transducer probes recalled to add useful life labelling
OMNI III TEE Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
OMNI III TEE Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2368-2025·2025-09-03
D5cwc ultrasound probes recalled for labelling defining device useful life
D5cwc Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
D5cwc Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2375-2025·2025-09-03
L12-5 38mm transducer probes recalled to add useful life labelling
L12-5 38mm Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L12-5 38mm Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2373-2025·2025-09-03
L12-4 transducer probes recalled to define ultrasound transducer useful life
L12-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L12-4 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2354-2025·2025-09-03
C5-2 Lumify transducer probes recalled to add useful life labelling
C5-2 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C5-2 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2359-2025·2025-09-03
C8-5 ultrasound probes recalled for labelling defining transducer useful life
C8-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C8-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2399-2025·2025-09-03
S9-2 transducer probes recalled to clarify useful life in the field
S9-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S9-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2358-2025·2025-09-03
C8-4v ultrasound transducer probes recalled to add useful life labelling
C8-4v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C8-4v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2408-2025·2025-09-03
X5-1 transducer probes recalled to clarify useful life in the field
X5-1 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
X5-1 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2380-2025·2025-09-03
L18-5 ultrasound transducer probes recalled to add useful life labelling
L18-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L18-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2347-2025·2025-09-03
3D9-3v ultrasound transducer probes recalled for useful life labelling clarification
3D9-3v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
3D9-3v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2392-2025·2025-09-03
S4-1 Lumify transducer probes recalled to define transducer useful life
S4-1 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S4-1 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2365-2025·2025-09-03
C9-5ec transducer probes recalled over useful life labelling clarification
C9-5ec Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C9-5ec Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2404-2025·2025-09-03
V9-2 transducer probes recalled to add useful life labelling
V9-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
V9-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2390-2025·2025-09-03
S3-1 transducer probes recalled over useful life labelling clarification
S3-1 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S3-1 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2350-2025·2025-09-03
C10-3v transducer probes recalled to define ultrasound transducer useful life
C10-3v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C10-3v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2387-2025·2025-09-03
OMNI II TEE transducer probes recalled over useful life labelling clarification
OMNI II TEE Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
OMNI II TEE Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide