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.

34476–34500 of 79559

CriticalFDA (Drugs)·D-0125-2020·2019-10-02
FDA Recalls Quinacrine Dihydrochloride Bulk API Due to Labeling Error
Darmerica, LLC is recalling 1.8 kilograms of bulk Quinacrine Dihydrochloride API because testing revealed the product was actually Artemisinin.
Product
Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55, c) 25g NDC# 71052-530-25, Darmerica LLC 198 Wilshire Blvd Casselberry, FL 32707
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1881-2019·2019-10-02
Johnson Matthey Recalls Cisplatin Active Pharmaceutical Ingredient Due to Glass Contamination
Johnson Matthey Inc. is recalling 26,625 grams of Cisplatin Active Pharmaceutical Ingredient due to potential glass contamination.
Product
Cisplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V698000·2019-10-02
BMW Recalls 2000-2002 Models for Driver Air Bag Inflator Defect
BMW is recalling 2000-2002 323, 325, and 330 models because the driver-side air bag inflator may explode, posing a risk of serious injury or death.
Product
BMW — BMW 330, 325, 323
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V696000·2019-10-02
Lamborghini Recalls 2017-2019 Aventador S Models Due to Engine Stall Risk
Lamborghini is recalling 441 Aventador S vehicles because engine software may cause the engine to stall when coasting to a stop, increasing crash risk.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR S, AVENTADOR S ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2552-2019·2019-10-02
Sentinel CH SpA Recalls Alinity c Lithium Reagent Kits
Sentinel CH SpA is recalling Alinity c Lithium Reagent Kits due to a potential carryover issue that may result in falsely elevated lithium patient results.
Product
Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V697000·2019-10-02
BMW Recalls 2020 S1000 RR Motorcycles Due to Oil Cooler Hose Defect
BMW is recalling 416 2020 S1000 RR motorcycles because oil cooler hoses may not be attached properly, potentially causing an oil leak that increases crash risk.
Product
BMW — BMW S1000 RR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2561-2019·2019-10-02
Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors
Elekta Inc is recalling 49 Monaco RTP Systems because unintentional changes to electron density settings may cause incorrect dose calculations for radiation therapy plans.
Product
Monaco RTP System, 5.50/5.51, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2756-2019·2019-10-02
Medline Electric Surgical Clipper Recalled for Overheating Charger Base
Medline Industries is recalling 500 electric surgical clippers because a defective circuit board component may cause the charger base to overheat and malfunction.
Product
MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V695000·2019-10-02
Daimler Recalls 2018-2019 Sprinter Vehicles for Inactive Airbag Systems
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because their airbag systems may not have been activated, increasing crash injury risk.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V693000·2019-10-02
Mercedes-Benz Recalls 2018-2019 Sprinter and Metris Vans for Safety Inspection
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vans because they left the reassembly plant without final quality inspection of safety-relevant parts.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2560-2019·2019-10-02
Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors
Elekta Inc is recalling 30 units of the Monaco RTP System 5.40 Unity because unintentional changes to electron density settings may result in incorrect dose calculations for radiation treatment plans.
Product
Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2556-2019·2019-10-02
Arrow Central Venous Catheterization Kit Recalled for Incorrect Banner Card
Arrow International Inc is recalling 231 units of 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kits because they may contain the incorrect banner card.
Product
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1876-2019·2019-10-02
Nucala Injection Recalled for Temperature Abuse During Storage and Shipping
Cardinal Health is recalling 38 syringes of Nucala (mepolizumab) because the product was stored and shipped outside of labeled temperature requirements.
Product
NUCALA — NUCALA (MEPOLIZUMAB)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2551-2019·2019-10-02
Sentinel CH SpA Recalls MULTIGENT Lithium Reagent Kits
Sentinel CH SpA is recalling 15,919 MULTIGENT Lithium reagent kits due to a potential carryover issue that may cause falsely elevated patient results.
Product
MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1882-2019·2019-10-02
FDA Recalls Oxaliplatin Active Pharmaceutical Ingredient Due to Glass Contamination
Johnson Matthey Inc. is recalling Oxaliplatin Active Pharmaceutical Ingredient due to potential glass contamination. The product was distributed nationwide in the United States.
Product
Oxaliplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001, NDC 49821-0075-XX
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2549-2019·2019-10-02
Philips Infant/Child Defibrillator Pads Recalled for Incorrect Age Labeling
Philips is recalling infant/child defibrillator pads due to incorrect age range labeling on the foil packaging.
Product
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Category
Medical Device
Distribution
51 states
ModerateFDA (Devices)·Z-2755-2019·2019-10-02
Abbott APS Accelerator Modules Recalled for Missing Pacemaker Safety Label
Abbott is recalling 159 APS Accelerator modular systems because the safety pacemaker label is missing. The Operations Manual has been updated to specify a 200 mm minimum safety distance for pacemaker wearers.
Product
APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,
Category
Medical Device
Distribution
21 states
ModerateFDA (Devices)·Z-2449-2019·2019-10-02
GE Healthcare Recalls Proteus XR/a Radiographic Systems for Audible Indicator Failure
GE Healthcare is recalling Proteus XR/a radiographic systems because they may fail to provide an audible indication when an exposure is complete.
Product
Proteus XR/a (SlOK : K993090)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2553-2019·2019-10-02
GN Otometrics Recalls Gold Cup and Snap Leadwires Due to Conductor Defect
GN Otometrics is recalling Gold Cup and Snap Leadwires because the electrode lead connector has a protruding conductor beyond the insulation.
Product
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap Leadwire, Blue; 3. 24" Snap Leadwire, Red; 4. 40" Snap Leadwire, Red; 5. 24" Snap Leadwire, Green; 6. 40" Snap Leadwire, Green…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2554-2019·2019-10-02
Smiths Medical Medfusion 4000 Syringe Infusion Pump Recall for Wireless Connectivity Issues
Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps with PharmGuard Server Software due to potential wireless network connectivity issues caused by a Radio Module defect.
Product
Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names: MEDFUSION¿ 4000 Pump V1.0; MEDFUSION¿ 4000 Pump V1.1, v1.1.1, v1.1.2; MEDFUSION¿ 4000 Pump V1.1, V1.1.1, V1.1.2; MEDFUSION¿ 4000 Pump V1.5, V1.5.1…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1880-2019·2019-10-02
Fentanyl Citrate Ingredient Recalled for Potential Glass Contamination
Johnson Matthey Inc. is recalling fentanyl citrate active pharmaceutical ingredient due to potential glass contamination.
Product
Fentanyl Citrate Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2754-2019·2019-10-02
Siemens Recalls Atellica IM Anti-CCP IgG Assay Due to Mitigation Failure
Siemens Healthcare Diagnostics is recalling 169 kits of the Atellica IM anti-CCP IgG assay because a reagent carryover mitigation step fails to complete on the analyzer.
Product
Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998 (100 Test) Test Version1.0 - Product Usage: The ADVIA Centaur¿ Anti-CCP IgG (aCCP) assay is for in vitro diagnostic use in the semi-quantitative determination of the IgG class of autoantibodies specific to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2753-2019·2019-10-02
Accu-Chek Connect App Recall for Android Data Transfer Failure
Roche Diabetes Care is recalling the Accu-Chek Connect App because users on Android OS 8.0 and above may be unable to transfer meter values to the app.
Product
Accu-Chek Connect Diabetes Management App
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1878-2019·2019-10-02
Akorn Recalls Lidocaine Hydrochloride Jelly Due to Metal Particulate Finding
Akorn, Inc. is recalling Lidocaine Hydrochloride Jelly USP, 2% due to a finding of metal particulate matter in the filling room. No particulates were identified in the product itself.
Product
Lidocaine Hydroclhoride Jelly USP, 2%, 30 mL tubes, Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-711-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2555-2019·2019-10-02
Arrow International Recalls Central Venous Access Kits Due to Incorrect Banner Card
Arrow International Inc is recalling 520 units of ARROW+gard Blue PSI Kit Cath-Gard central venous access devices because they may contain the incorrect banner card.
Product
8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A - Product Usage: The MACTM Two-Lumen Central Venous Access Device with ARROWg+ard Blue¿ permits venous access and catheter introduction to the central circulation. It…
Category
Medical Device
Distribution
Distributed nationwide