State

Kansas product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35726–35750 of 79559

ModerateFDA (Devices)·Z-1916-2019·2019-07-10
Siemens SOMATOM go.Now CT Scanner Recall for Workflow Interruptions
Siemens Medical Solutions is recalling 53 SOMATOM go.Now CT scanners due to potential sporadic performance problems that may cause scanning workflow interruptions and delays in diagnosis.
Product
SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1920-2019·2019-07-10
Siemens SOMATOM go.Now CT Systems Recalled for Performance Issues
Siemens is recalling 69 SOMATOM go.Now CT systems due to potential performance problems that may cause diagnostic delays or the need for patient rescans.
Product
SOMATOM go.Now, Model No. 11061618 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2019·2019-07-10
Zimmer Biomet Recalls DVR Crosslock ePAK Screw Drivers Due to Packaging Seal Risk
Zimmer Biomet is recalling 3,022 DVR Crosslock ePAK Screw Drivers because sterile packaging seals may be weak, potentially compromising sterility.
Product
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1917-2019·2019-07-10
Siemens SOMATOM go.All CT Systems Recalled for Performance Issues
Siemens is recalling 24 SOMATOM go.All CT systems due to sporadic performance problems that may interrupt scanning workflows and delay diagnoses.
Product
SOMATOM go.All (Model #11061630), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1948-2019·2019-07-10
Zimmer Biomet Recalls K-Wire Trochar Tips Due to Packaging Seal Issues
Zimmer Biomet is recalling K-Wire Trochar Tips because the sterile packaging may have weak seals, potentially compromising the device's sterility.
Product
K-Wire Trochar Tip, Model Number 212000008 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1906-2019·2019-07-10
Bio-Rad Recalls EVOLIS Microplate System Due to Software Error
Bio-Rad is recalling 213 EVOLIS Microplate Systems because a software defect may cause erroneous test results to be transmitted to laboratory information systems.
Product
EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management Software, (Catalog no. 90471A.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1932-2019·2019-07-10
Medtronic Recalls 0-arm 1000 Imaging Systems Due to Charger Board Defect
Medtronic is recalling 832 0-arm 1000 Imaging Systems worldwide because a defective charger board prevents batteries from fully recharging, rendering the system inoperable.
Product
Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and B1-700-00028-XXX (where XXX indicates the system voltage): Product Name Model#/ CFN OARM ASSY 8170000027 SYSTEM PRODUCT BI70000027 OARM ASSY BI70000027R SYS PRODUCT RWK BI70000027R BASE OARM 8170000027100 SYSTEM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1454-2019·2019-07-10
InvaGen Recalls Testosterone Topical Solution Due to Defective Container
InvaGen Pharmaceuticals is recalling 1,776 bottles of Testosterone Topical Solution because defective containers may cause the actuator to function improperly, affecting dose delivery.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1947-2019·2019-07-10
Zimmer Biomet Recalls DVR Crosslock ePAK Depth Gauges for Packaging Defects
Zimmer Biomet is recalling DVR Crosslock ePAK Depth Gauges due to a potential for weak seals in the sterile packaging.
Product
DVR Crosslock ePAK Depth Gauge, Model Number 212000003 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1918-2019·2019-07-10
Siemens SOMATOM go.Top CT Systems Recalled for Performance Issues
Siemens Medical Solutions is recalling 30 SOMATOM go.Top CT systems due to potential performance problems that may interrupt scanning workflows and delay patient diagnoses.
Product
SOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1937-2019·2019-07-10
Beckman Coulter iChem VELOCITY Urine Strips Recalled for False Positives
Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Strips because increased sensitivity causes falsely elevated urobilinogen results.
Product
iChem VELOCITY Urine Chemistry Strips, REF 800-7212, 100 test strips/vial. The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland, Made in Germany.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1921-2019·2019-07-10
Siemens SOMATOM go.All CT Scanner Recalled for Performance Issues
Siemens is recalling 69 SOMATOM go.All CT scanners due to potential performance problems that may cause diagnostic delays or require patient rescans.
Product
SOMATOM go.All, Model No. 11061638 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2019·2019-07-10
Phadia EliA RF IgM Well Recalled for Potential Low Assay Results
Phadia Ab is recalling EliA RF IgM Well kits due to a potential for reporting low assay results, which may affect rheumatoid arthritis diagnosis.
Product
EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid factor antibodies in human serum and plasma (Li-heparin and EDTA) to aid in the diagnosis of rheumatoid arthritis in conjunction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1922-2019·2019-07-10
Siemens CT System Recalled for Potential Scanning Workflow Interruptions
Siemens Medical Solutions is recalling 69 SOMATOM go.Top CT systems due to potential sporadic performance problems that may cause diagnostic delays or the need for patient rescans.
Product
SOMATOM go.Top, Model No. 11061648 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1438-2019·2019-07-10
Amneal Recalls Subpotent Esterified Estrogens and Methyltestosterone Tablets
Amneal Pharmaceuticals is recalling specific lots of Esterified Estrogens & Methyltestosterone tablets due to out-of-specification assay results.
Product
Esterified Estrogens & Methyltestosterone Tablets, USP 0.625 mg/1.25 mg, 100-count bottles, Rx Only, Manufactured by: Ammeal Pharmaceuticals of NY Hauppauge, NY 11788 Distributed by: Seton Pharmaceuticals Manasquan, NJ 08736, NDC 13925-171-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1927-2019·2019-07-10
Roche cobas p 501 Post-Analytical Units Recalled for Loose Flap
Roche Diagnostics is recalling four cobas p 501 post-analytical units because the tray input flap may become loose and detach from the instrument.
Product
cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1439-2019·2019-07-10
Amneal Recalls Subpotent Esterified Estrogens and Methyltestosterone Tablets
Amneal Pharmaceuticals is recalling specific lots of Esterified Estrogens & Methyltestosterone Tablets because they failed potency testing.
Product
Esterified Estrogens & Methyltestosterone Tablets, USP 1.25 mg/2.5 mg, 100-count bottles, Rx Only, Manufactured by: Ammeal Pharmaceuticals of NY Hauppauge, NY 11788 Distributed by: Seton Pharmaceuticals Manasquan, NJ 08736, NDC 13925-172-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1928-2019·2019-07-10
Roche cobas p 701 Post-Analytical Units Recalled for Loose Flap
Roche Diagnostics is recalling nine cobas p 701 post-analytical units because the tray input flap may become loose and detach.
Product
cobas p 701 post-analytical units, Part Number 05349966001. For diagnostic sample storage and retrieval.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V516000·2019-07-09
Jayco Recalls 2019-2020 White Hawk Travel Trailers Due to Brake Wiring Defect
Jayco is recalling 2019-2020 White Hawk travel trailers because incorrectly wired breakaway switches may prevent trailer brakes from functioning if the trailer separates from the tow vehicle.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19758·2019-07-09
Swaddle Bee Recalls Loviebee Children's Security Blankets Due to Choking Hazard
Swaddle Bee is recalling about 700 Loviebee children's security blankets because metal snaps can detach, posing a choking hazard. No injuries have been reported.
Product
Loviebee children's security blankets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19159·2019-07-08
Disney Recalls Forky Plush Toys Due to Choking Hazard
Disney is recalling approximately 80,000 Forky plush toys because the plastic eyes can detach, posing a choking hazard to young children.
Product
Forky 11" Plush Toys
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V515000·2019-07-05
Ford Recalls Focus Vehicles Due to Potential Engine Stall Risk
Ford is recalling certain 2012-2017 Focus vehicles because a malfunctioning valve may cause the engine to stall while driving, increasing crash risk.
Product
FORD — FORD FOCUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V514000·2019-07-05
Mazda Recalls 2019 Mazda3 Vehicles Due to Head Restraint Defect
Mazda is recalling 2019 Mazda3 vehicles because seat cover material may prevent front head restraints from locking properly, increasing injury risk in a crash.
Product
MAZDA — MAZDA MAZDA3
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1385-2019·2019-07-03
Vyaire Medical Recalls enFlow Cartridges Due to Aluminum Elution
Vyaire Medical is recalling enFlow Disposable Cartridges because testing showed aluminum elution during fluid warming. The recall covers 5,782,820 units distributed worldwide.
Product
enFlow Disposable Cartridge, used for intravenous warming therapy with fluid and blood solutions.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1427-2019·2019-07-03
Premier Pharmacy Labs Recalls Succinylcholine Chloride Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling 6,423 syringes of Succinylcholine Chloride due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
SUCCINYLcholine Chloride, 100mg/5mL (20mg/mL), 5mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-239-15, barcode 0 69623 23915 0.
Category
Drug
Distribution
Distributed nationwide