State

Missouri product recalls

73,737 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,500
Critical: 1,339
Severe: 2,203
Most recent: 2026-10-28

Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32051–32075 of 82237

HighFDA (Devices)·Z-1861-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling specific Hemashield Gold vascular grafts due to potential small holes at the seam lines that may cause intra-operative bleeding.
Product
Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product Code: M002020955890 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V272000·2020-05-13
Audi Recalls 2020 Q8 Models for Transmission Fluid Leak Risk
Volkswagen is recalling 2020 Audi Q8 vehicles because a defective transmission oil pipe may leak fluid, making roads slippery and increasing crash risk.
Product
AUDI — AUDI Q8
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1898-2020·2020-05-13
NuVasive MAGEC 2 Spinal Rods Recalled for Actuator Separation
NuVasive Inc. is recalling MAGEC 2 spinal rods because actuator end caps may separate, exposing internal components and releasing titanium wear debris.
Product
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1862-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175426T0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1867-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175734P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1876-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling specific Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1869-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Defects
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175822P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Defects
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175830P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175922P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Line Holes
Maquet Cardiovascular is recalling specific Hemashield Gold vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2020·2020-05-13
CME America Recalls BodyGuard Microset Infusion Sets Due to Filter Defect
CME America is recalling BodyGuard Microset infusion sets because the installed filter may have the incorrect pore size. The recall affects 30,300 units distributed nationwide.
Product
BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stripe - Product Usage: The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1872-2020·2020-05-13
Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20120·2020-05-13
Hodedah Recalls 4-Drawer Chests Due to Tip-Over and Entrapment Hazards
Hodedah is recalling HI4DR 4-drawer chests because they may tip over or entrap children if not anchored to the wall.
Product
Hodedah HI4DR 4-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V269000·2020-05-13
2020–2021 Forest River Vibe Trailers Recalled for Missing Refrigerator Roof Vent
Forest River is recalling certain 2020–2021 Vibe trailers because the roof vent for the refrigerator may be missing. Without proper ventilation, the refrigerator could overheat and create a fire risk, or carbon monoxide could accumulate inside the trailer.
Product
FOREST RIVER — FOREST RIVER VIBE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Defects
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1926-2020·2020-05-13
Stryker Recalls Spy-Phi Drapes Packaged in Unsealed Pouches
Stryker is recalling 21,078 units of Spy-Phi Drapes because they were packaged in unsealed pouches, compromising sterility.
Product
Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally only). Drape/ UDI: HH2020/20858701006326
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2020·2020-05-13
Intuitive Surgical Recalls daVinci XI Sureform Stapler Reloads Due to Deployment Defect
Intuitive Surgical is recalling 22,752 daVinci XI Sureform 60 reloads worldwide because a manufacturing variation may prevent adjacent staples from deploying, potentially causing an incomplete staple line.
Product
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic…
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·010-2020·2020-05-13
Evans Food Group Recalls Pork Skin Products Due to Undeclared Soy
Evans Food Group is recalling ready-to-eat pork skin products because the variety pack label fails to declare soy, a known allergen.
Product
Evans Food Group — Evans Food Group Recalls Ready-To-Eat Pork Skin Products due to Misbranding
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1882-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1899-2020·2020-05-13
Varian Multileaf Collimator Recall Due to Software-Related Leaf Movement Failure
Varian Medical Systems is recalling 151 Multileaf Collimators because a software upgrade caused leaves to fail to move during specific arc treatments.
Product
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf Collimator Model Number(s): product code: H54 and H56; MLC software version 8.5 - Product Usage: is intended to assist the clinician in the delivery of external…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1841-2020·2020-05-13
Philips Recalls Transesophageal Ultrasound Transducers Due to Temperature Measurement Failure
Philips Ultrasound Inc is recalling S7-3t transesophageal transducers because a manufacturing programming error prevents the system from correctly measuring tip temperature, which may stop auto-cooling and cause patient injury.
Product
Transducer S7-3t UDI (01)00884838061439 REF 989605406772 Can be used with: CX50, EPIQ 7, Affiniti 50 and Affiniti 70 Ultrasound systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2020·2020-05-13
Ivoclar Vivadent recalls dental ceramic blocks due to cracking during sintering
Ivoclar Vivadent AG is recalling 332 units of IPS e.max ZirCAD ceramic blocks because they crack during the sintering process. The recall covers lots Y47472 and Z000V0 distributed nationwide.
Product
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - ceramic for dental use,intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/ CAM technology Product Number: 686194
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2020·2020-05-13
Inpeco Centrifuge Module Recall for Potential Unbalanced Load Damage
Inpeco S.A. is recalling 23 Abbott Accelerator a3600 Centrifuge Modules because a loading algorithm defect may cause unbalanced loads that could damage the equipment.
Product
Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
Category
Medical Device
Distribution
27 states
HighFDA (Devices)·Z-1864-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide