State

Missouri product recalls

73,833 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,501
Critical: 1,339
Severe: 2,204
Most recent: 2026-11-04

Of the 8,501 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 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55176–55200 of 82334

HighFDA (Devices)·Z-1281-2016·2016-04-06
Siemens Recalls Cios Alpha X-Ray Systems Due to Electrical Shock Risk
Siemens is recalling four Cios Alpha mobile X-ray systems because a defective part could increase the risk of electrical shock for service personnel during maintenance.
Product
CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The Cios Alpha is a mobile X-ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but are not limited to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1301-2016·2016-04-06
Siemens CT Systems Recalled for Potential Malfunction Hazard
Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.
Product
Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1288-2016·2016-04-06
Ossur Recalls Multiple Medical Devices Including Miami J Collars
Ossur Americas is recalling various medical devices, including Miami J collars and knee shields, due to a manufacturing defect.
Product
Miami J Collar Product Usage: Miami J collars are applied to patients afflicted with cervical injuries to ensure immobilization.
Category
Medical Device
Distribution
48 states
HighFDA (Devices)·Z-1257-2016·2016-04-06
ICU Medical Recalls I.V. Infusion Sets with Potential Leak
ICU Medical is recalling specific I.V. infusion administration sets because a connection may develop a leak. The recall affects 350 units distributed in the US and internationally.
Product
110" (279 cm) Appx 13.8 ml, 20 Drop Admin Set w/ Integrated ChemoLock Port Drip Chamber, Clave, Rotating Luer, Bag Hanger, Item No. AHCL3300 sterile devices intended for the infusion and withdrawal of fluids.
Category
Medical Device
Distribution
14 states
ModerateFDA (Devices)·Z-1297-2016·2016-04-06
Ossur Recalls Multiple Medical Devices Including Knee Braces and Walkers
Ossur Americas is recalling various medical devices, including knee braces and walkers, due to unspecified product issues.
Product
Extreme Custom Product Usage: Extreme Custom is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
Category
Medical Device
Distribution
48 states
ModerateFDA (Devices)·Z-1280-2016·2016-04-06
Philips Medical Systems Recalls Foot Switches for Bent Pedal Defect
Philips Medical Systems is recalling 4,180 foot switches used with Allura Xper systems because a bent pedal can cause loss of key image functionality.
Product
Foot Switches used with the following systems: Philips Allura Xper Systems; 722001 AlluraXperFDlO C, 722002 Allura Xper FD1O F, 722003 Allura Xper FD1O, 722005 Allura Xper FD1O/10, 722006 Allura Xper FD2O, 722008 Allura Xper FD2O Biplane, 722010 Allura Xper FD1O, 722011 Allura…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0812-2016·2016-04-06
Ventura Foods Recalls 35 lb. Liquid Fry Shortening Due to Plastic Contamination
Ventura Foods is recalling various brands of 35 lb. liquid fry shortening because plastic from the jugs may have entered the product.
Product
45532-ATL : Atlantic Food Distributors Premium Clear Liquid Fry Shortening 35 lb. ; 45531-ATL : Atlantic Food Distributors Premium Creamy Liquid Fry Shortening 35 lb. ; 45531-CHP : Chef's Pride Creamy Liquid Fry Shortening 35 lb. ; 45531-UBA : Creamy Liquid Fry Shortening 35…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1249-2016·2016-04-06
Medtronic Recalls Reveal LINQ Cardiac Monitor Due to Algorithm Sensitivity Issue
Medtronic is recalling Reveal LINQ insertable cardiac monitors because an algorithm issue may trigger replacement alerts prematurely. The device battery and data collection capabilities remain functional.
Product
Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1267-2016·2016-04-06
Implant Direct Sybron Recalls GoDirect Dental Implants Due to Tool Error
Implant Direct Sybron is recalling GoDirect Implants because some consignees received the wrong tool to drive the implant to bone level.
Product
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that compose a two-piece implant system. GoDirect Implants Part Number: 423011, 423013, 424708, 424710, 424713,433010,433710
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1311-2016·2016-04-06
Siemens Artis zee/zeego X-Ray Systems Recalled for Cooling System Leak
Siemens is recalling 1,757 Artis zee/zeego angiographic X-ray systems because a possible leak in the cooling system could allow fluids to seep into the equipment cabinet.
Product
Artis zee/zeego (system, x-ray, angiographic) for single and biplane diagnostic imaging and interventional procedures such as cardiac and neuro angiography, general and rotational angiography, operating room angiography, multipurpose angiography and whole body…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0999-2016·2016-04-06
ProSupps Recalls Mr. Hyde Pre-Workout for Undeclared Picamilon Ingredient
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
Product
Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS ORANGE BURST NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 4.0 OZ (113 GRAMS) and Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 30 SERVINGS ORANGE BURST NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT NET…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0813-2016·2016-04-06
Ventura Foods Recalls Cooking Oil Jugs Due to Plastic Contamination
Ventura Foods is recalling 35 lb. jugs of cooking oil because plastic fragments may be present due to a manufacturing defect in the jugs.
Product
45532-CHP: Chef's Pride Soybean Clear Fry Oil 35 lb.; 54135-CHP: Chef's Pride Soybean Salad Oil 35 lb.; 45635-CHP: Chef's Pride Soybean Pan & Grill Frying Oil 35 lb.; 54135-TXR: Texas Roadhouse Soybean Salad Oil 35 lb.; 54135-PAD: Panda Express Soybean Salad Oil 35 lb.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1262-2016·2016-04-06
Siemens E.CAM Gamma Camera Recall for Collimator Change Instructions
Siemens is recalling 3,090 E.CAM gamma camera systems to provide supplemental instructions and visual aids for proper collimator changes.
Product
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the distribution of radiopharmaceuticals in humans for the purpose of determining various metabolic (molecular) and physiologic functions within the human body
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1253-2016·2016-04-06
Biomet Spine Recalls Solitaire Ti Spacers Due to Mislabeled Lordotic Angle
Biomet Spine is recalling specific Solitaire Ti Spacers because they are mislabeled as having a 12-degree lordotic angle when the actual angle is 6 degrees.
Product
10mm X 12o Solitaire Ti Medium Spacer Solitaire Anterior Spinal System, Model Number 1400-1230. Product Usage: The SOLITAIRETM SPINAL SYSTEM is designed for use with autograft and is indicated for stand-alone intervertebral body fusion at one level or two contiguous levels…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1282-2016·2016-04-06
Siemens Artis One X-Ray System Recalled for Data Mirroring Error
Siemens is recalling one Artis One angiography system because imported left atrium segmentation results may be incorrectly mirrored to a 3D mapping system.
Product
Artis One, Interventional, Fluoroscopic, x-ray system Artis one is an angiography system developed for diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis One include…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1263-2016·2016-04-06
Siemens Symbia Gamma Camera Recall for Collimator Change Instructions
Siemens is recalling 726 Symbia gamma camera systems worldwide to provide supplemental instructions clarifying the proper collimator change procedure.
Product
The Symbia gamma camera system Product Usage: The Symbia gamma camera system is a computed tomography x-ray system which is a diagnostic x-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0782-2016·2016-04-06
Praxair Recalls 127 Cylinders of Compressed Medical Air Due to Odor
Praxair Inc. is recalling 127 cylinders of compressed medical air because a customer reported an odor when turning on a cylinder.
Product
UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0814-2016·2016-04-06
Ventura Foods Recalls Canola Frying Oil Due to Plastic Contamination
Ventura Foods is recalling 35 lb. jugs of canola frying oil because plastic from the jug's sealing surface may have been pushed into the product during manufacturing.
Product
18159-BLN : Brilliance Clear Zero Premium Clear Canola Frying Oil 35 lb. ; 58503-CHP : Chef's Pride Canola Clear Fry Oil 35 lb. ; 58503-FLV : Flavorite Canola Clear Fry Oil 35 lb. ; 58503-PLF : Planet Fry Canola Clear Fry Oil 35 lb. ; 58503-NGT : Nugget Brand Canola Clear…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1279-2016·2016-04-06
Philips MultiDiagnost Eleva Foot Switches Recalled for Bent Pedal Defect
Philips Medical Systems is recalling 168 foot switches used with the MultiDiagnost Eleva system because a bent pedal can cause loss of key image functionality.
Product
Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 This Philips MultiDiagnost Eleva is intended to be used as a multifunctional/universal system. General RIF, Fluoroscopy, Radiography and Angiography can be performed along with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1001-2016·2016-04-06
ProSupps Recalls Mr. Hyde Pre-Workout for Undeclared Picamilon Ingredient
ProSupps USA LLC is recalling 33 units of Mr. Hyde Intense Energy Pre-Workout because the product may contain undeclared Picamilon.
Product
Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS BLUERAZZ NATURAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 3.7 OZ (105 GRAMS) packaged in red plastic jars with black lids.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1252-2016·2016-04-06
Molteno3 Glaucoma Implants Recalled for Updated Instructions
Innovative Ophthalmic Products is recalling Molteno3 Glaucoma Implants because the package insert was updated to add a caution statement to minimize off-label use.
Product
Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#: M3-175) GL-Single Plate 230mm2 (IOP reorder#: M3-230)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1268-2016·2016-04-06
Pelton & Crane Recalls Helios Track Mounted Dental Lights
Pelton & Crane is recalling 156 Helios HL3T and HLT track mounted dental lights because they were missing two set screws during initial installation.
Product
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1264-2016·2016-04-06
Wfr/aquaplast Recalls Prone Breast Treatment Tables Due to Scale Misalignment
Wfr/aquaplast Corp is recalling 30 prone breast treatment tables and devices because some may have misaligned scales, potentially causing orientation differences.
Product
Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device Product Usage: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device is a medical charged-particle radiation therapy system. A breast radiation therapy patient…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1285-2016·2016-04-06
Ossur Recalls Knee Shields and Medical Devices Due to Packaging Defect
Ossur Americas is recalling various medical devices, including knee shields and walkers, because the packaging is defective.
Product
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide protection from debris or impact to the patella while a patient participates in motocross activities.
Category
Medical Device
Distribution
48 states
LowFDA (Drugs)·D-0783-2016·2016-04-06
Praxair Recalls Medical Air Cylinders Due to Odor Complaint
Praxair Inc. is recalling 382 cylinders of medical air nationwide after a customer reported an odor when turning on a cylinder.
Product
UN1002 Air, Compressed, Medical Air, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113,
Category
Drug
Distribution
Distributed nationwide