State

Kansas product recalls

72,936 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,723
Critical: 1,045
Severe: 1,228
Most recent: 2026-09-02

Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (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 5,723 recalls whose distribution notice names Kansas specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2576–2600 of 78659

HighFDA (Devices)·Z-1655-2026·2026-04-08
Paradise renal denervation catheter distributed despite being marked for scrapping
Recor Medical is recalling one lot of the Paradise Ultrasound Renal Denervation System Catheter because a nonconforming product that should have been scrapped was distributed instead.
Product
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0413-2026·2026-04-08
GoodSense original formula eye drops recalled over sterility assurance
GoodSense Eye Drops Original Formula, containing tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
GOODSENSE EYE DROPS ORIGINAL FORMULA — GOODSENSE EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1710-2026·2026-04-08
Medline bronchoscopy kits contain Olympus biopsy valves that shed fragments
Medline is recalling six bronchoscopy and thoracic kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I 5. KIT, WR THORACIC, DYNJ911252 6. LARYNGOSCOPY/BRON
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2026·2026-04-08
Oxoid Microbact Listeria kit may identify the incorrect organism
Oxoid, part of Thermo Fisher Scientific, is recalling one lot of the Microbact 12L Listeria identification kit because it may identify the incorrect organism.
Product
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0410-2026·2026-04-08
Quality Choice moisturizing relief eye drops recalled over sterility assurance
Quality Choice Moisturizing Relief Eye Drops, containing dextran 70, polyethylene glycol 400, povidone and tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS — QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2026·2026-04-08
MiniMed 630G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 630G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1747-2026·2026-04-08
MiniMed 620G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 620G Insulin Pump (MMT-1750)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2026·2026-04-08
Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2026·2026-04-08
Medline ENFit G-tube connector kits may leak from dimensional defect
Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.
Product
Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1705-2026·2026-04-08
Airway exam kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling the Airway Exam Kit because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Airway Exam Kit, DYKE1796
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2026·2026-04-08
Burlington Medical half aprons may lose radiation attenuation over time
Burlington Medical is recalling half aprons because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Half Aprons.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2026·2026-04-08
Olympus SOLTIVE Premium laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Premium SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2026·2026-04-08
VOLT locking screw taps swapped between lots carry incorrect thread
The 2.4 VOLT Tap Locking Screw Tap is being recalled after a full lot swap with the Cortical Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1682-2026·2026-04-08
CPX 4 low height tissue expander infusion needles may be blunt
Mentor is recalling the CPX 4 US Breast Tissue Expander with Suture Tabs, smooth low height 650 cc, because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH Smooth Low Height Tissue Expander, 650cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1703-2026·2026-04-08
VOLT bone taps swapped between lots carry the incorrect thread
The 2.4 VOLT Tap Cortex Screw is being recalled after a full lot swap with the VOLT Locking Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2026·2026-04-08
MiniMed 670G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2026·2026-04-08
CPX 4 medium height tissue expander infusion needles may be blunt
Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth medium height range because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2026·2026-04-08
MiniMed 780G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 780G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1674-2026·2026-04-08
Philips Azurion 3 M15 X-ray may not start from foot switch
Philips is recalling the Azurion 3 M15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0419-2026·2026-04-08
Prazosin hydrochloride 100-count bottles recalled over nitrosamine impurity
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1665-2026·2026-04-08
Philips Allura Xper FD20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0412-2026·2026-04-08
Leader ultra lubricating eye drops recalled over sterility assurance failure
Leader Ultra Lubricating Eye Drops, containing polyethylene glycol 400 and propylene glycol, are being recalled for lack of assurance of sterility.
Product
LEADER ULTRA LUBRICATING EYE DROPS — LEADER ULTRA LUBRICATING EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0421-2026·2026-04-08
Prazosin hydrochloride further lots recalled over nitrosamine impurity levels
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide