State

Missouri product recalls

72,933 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,461
Critical: 1,333
Severe: 1,870
Most recent: 2026-09-09

Of the 8,461 recalls naming Missouri we have scored against our rubric, 1,333 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.

Which agencies issued them

These figures cover only the 8,461 recalls whose distribution notice names Missouri specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2626–2650 of 81394

HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
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 (Devices)·Z-1670-2026·2026-04-08
Philips Allura Xper FD20/20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20 OR Table; System Code: 722039;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1753-2026·2026-04-08
Burlington Medical thyroid shields may lose radiation attenuation over time
Burlington Medical is recalling thyroid shields over the potential for attenuation degradation over time, which decreases the product's usable lifespan. 41,962 units are affected.
Product
Burlington Medical, Thyroid Shield.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1745-2026·2026-04-08
MiniMed 720G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1744-2026·2026-04-08
MiniMed 700G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 700G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1696-2026·2026-04-08
da Vinci monopolar curved scissors recalled over frayed grip cables
Intuitive Surgical is recalling da Vinci S and Si Monopolar Curved Scissors Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0408-2026·2026-04-08
Amneal tramadol tablets failed nitrosamine impurity specification at stability
Amneal Pharmaceuticals is recalling two lots of Tramadol Hydrochloride Tablets 50 mg after a nitrosamine impurity was found out of specification at the 24-month stability interval.
Product
TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1654-2026·2026-04-08
Paradise renal denervation catheter unit distributed despite scrapping designation
One Paradise Ultrasound Renal Denervation catheter was distributed although it was a nonconforming product that should have been scrapped and not used in humans.
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-1749-2026·2026-04-08
Paradigm REAL-Time insulin pump delivery varies with pump height
Medtronic is recalling Paradigm REAL-Time insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
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-1671-2026·2026-04-08
Philips Allura Xper FD20/15 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15; System Code: 722058;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2026·2026-04-08
Artoura breast tissue expander infusion set needles may be blunt
Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1687-2026·2026-04-08
Artoura ultra high profile expander infusion needles may be blunt
Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0660-2026·2026-04-08
Imu-Tek Colostrum-5 Capsules Recalled for Potential Under-Processing
Imu-Tek Animal Health is recalling Imu-Tek Colostrum-5 120 Capsules (Lot #013, Expiration 092826) because the product is potentially under-processed. The product was distributed across 29 states.
Product
Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524.
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-1657-2026·2026-04-08
Atellica hemoglobin A1c assay may return depressed patient results
Siemens is recalling Atellica CH Enzymatic Hemoglobin A1c because results may be depressed when the RCRP reagent is processed on the same analyzer, with bias increasing over time.
Product
Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1659-2026·2026-04-08
Philips Allura Xper FD10C X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD10C; System Code: 722001;
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 (Drugs)·D-0414-2026·2026-04-08
GNP redness and dry eye relief drops recalled over sterility assurance
GNP Eye Drops Redness and Dry Eye Relief, containing glycerin and naphazoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
LEADER EYE DROPS REDNESS RELIEF — LEADER EYE DROPS REDNESS RELIEF (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1663-2026·2026-04-08
Philips Allura Xper FD20 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1692-2026·2026-04-08
Vue Motion V12 may display cine image frames out of sequence
Philips is recalling Vue Motion V12 because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence.
Product
Vue Motion V12. Product Number: 1017979.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2026·2026-04-08
Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments
Medline is recalling four bronchoscopy and laryngoscopy 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. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1664-2026·2026-04-08
Philips Allura Xper FD20 Biplane X-ray may not start reliably
Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2026·2026-04-08
MiniMed 640G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 640G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0416-2026·2026-04-08
Leader artificial tears 15 mL recalled over sterility assurance failure
Leader Artificial Tears 15 mL, containing polyvinyl alcohol and povidone, are being recalled for lack of assurance of sterility.
Product
LEADER ARTIFICIAL TEARS 15 ML — LEADER ARTIFICIAL TEARS 15 ML (POLYVINYL ALCOHOL, POVIDONE)
Category
Drug
Distribution
Distributed nationwide