State

Missouri product recalls

73,104 recalls have nationwide distribution and so reach Missouri. 8,493 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,493
Critical: 1,344
Severe: 1,882
Most recent: 2026-09-23

Of the 8,493 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (22%) are Severe.

Which agencies issued them

These figures cover only the 8,493 recalls whose distribution notice names Missouri specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12101–12125 of 81597

ModerateFDA (Devices)·Z-2122-2024·2024-05-29
GMAX Blue Syringes Recalled for Out-of-Range Design Configurations
Jiangsu Shenli Medical recalled 9,800 GMAX blue syringes because their sizes and configurations fall outside FDA's clearance range. Affected units were distributed nationwide to healthcare facilities and retailers.
Product
Brand Name: GMAX Product Name: SYR 10ML/LL Blue syringe Model/Catalog Number: TS2210B-M Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2087-2024·2024-05-29
MEDLINE 5ML Non-Sterile Syringes Recalled for Unapproved Configurations
MEDLINE non-sterile syringes (Model 91859) are being recalled because their sizes and configurations exceed the scope of the manufacturer's FDA 510(k) clearance. No illnesses or injuries have been reported.
Product
Brand Name: MEDLINE Product Name: SYR 5ML L/L PURPLE NITRO Model/Catalog Number: 91859 Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0504-2024·2024-05-29
Prescription Drug Sirolimus Recalled for Failed Impurity Specifications
Dr. Reddy's Laboratories is recalling Sirolimus 1mg tablets nationwide due to failed impurity and degradation specifications. The recall affects 1,176 bottles from lot H2200493 expiring 6/30/2025.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2120-2024·2024-05-29
GMAX SYR 60ML/LS Syringes Recalled for Non-Approved Specifications
Jiangsu Shenli Medical is recalling GMAX SYR 60ML/LS syringes (Model TS2260S-M) because the piston syringe sizes and configurations exceed what was approved by FDA in the company's 510(k) clearance.
Product
Brand Name: GMAX Product Name: SYR 60ML/LS syringe Model/Catalog Number: TS2260S-M Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2118-2024·2024-05-29
FDA Recalls GMAX Syringes Due to Unapproved Configuration
Jiangsu Shenli is recalling GMAX 12ML syringes because the device sizes and configurations exceed what was cleared by FDA. Approximately 303,800 units were distributed nationwide.
Product
Brand Name: GMAX Product Name: SYR 12ML/LS syringe Model/Catalog Number: TS2212S-M Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2047-2024·2024-05-29
Medline Non-Sterile Syringes Recalled for Exceeding FDA-Cleared Specifications
Jiangsu Shenli Medical is recalling about 38.8 million Medline SYR 10ML L/L non-sterile syringes (Model 83082) because their sizes and configurations exceed FDA-cleared specifications. Nationwide distribution in CA, FL, GA, IL, TN, and VA.
Product
Brand Name: MEDLINE Product Name: SYR 10ML L/L Model/Catalog Number: 83082 Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2045-2024·2024-05-29
MEDLINE SYR 60ML Non-Sterile Syringes Recalled for Clearance Violation
Jiangsu Shenli Medical is recalling 1,117,800 MEDLINE SYR 60ML non-sterile syringes (Model 83080) because certain syringe sizes and configurations exceed what was approved under the manufacturer's FDA 510(k) clearance.
Product
Brand Name: MEDLINE Product Name: SYR 60ML L/L Model/Catalog Number: 83080 Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2102-2024·2024-05-29
Wolf Medical 3 mL Syringes Recalled for Out-of-Specification Manufacturing
Jiangsu Shenli Medical is recalling 777,400 Wolf Medical 3 mL syringes (Model SYR03L) manufactured outside FDA clearance scope. Users should discontinue use of affected lot codes.
Product
Brand Name: Wolf Medical Product Name: 3 mL (cc) Luer Lock STERILE LATEX FREE NON PYROGENIC Model/Catalog Number: SYR03L Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2064-2024·2024-05-29
Non-Sterile Syringes Recalled Outside FDA-Cleared Size and Configuration Range
Medline is recalling 820,400 non-sterile syringes (model 91832) because their sizes and configurations fall outside what was cleared by the FDA. The devices were not manufactured within the approved specifications.
Product
Brand Name: MEDLINE Product Name: SYR 10ML L/L BLUE Model/Catalog Number: 91832 Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2103-2024·2024-05-29
Wolf Medical Syringes Recalled for Uncleared Size and Configuration Variants
Jiangsu Shenli Medical is recalling Wolf Medical 6 mL syringes because certain variants weren't cleared under the 510(k). Approximately 454,400 units distributed nationwide are affected.
Product
Brand Name: Wolf Medical Product Name: 6 mL (cc) Luer Lock STERILE LATEX FREE NON PYROGENIC Model/Catalog Number: SYR06L Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2115-2024·2024-05-29
GMAX SYR 35ML Non-Sterile Syringes Recalled for Regulatory Non-Compliance
The FDA is recalling GMAX SYR 35ML/LL non-sterile syringes because the device specifications exceed what the manufacturer had FDA clearance to produce. No illnesses have been reported.
Product
Brand Name: GMAX Product Name: SYR 35ML/LL syringe Model/Catalog Number: TS2235L-M Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1889-2024·2024-05-29
Cerene Cryotherapy Device recall: missing error code in troubleshooting table
Channel Medsystems is recalling the Cerene Cryotherapy Device because error code 003 is missing from the device's troubleshooting documentation, which could prevent clinicians from properly diagnosing errors during use.
Product
Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number: FGS-7000 Product Description: The Cerene Cryotherapy Device is an endometrial ablation device that uses nitrous oxide (N2O) to freeze and ablate the endometrium to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2078-2024·2024-05-29
Medline Non-Sterile Syringes Recalled for Unapproved Configuration
Medline 10mL non-sterile syringes have been recalled because their piston size and configuration fall outside the range cleared by FDA. The recall affects 7,000 units distributed nationwide.
Product
Brand Name: MEDLINE Product Name: SYR 10ML L/L BLUE SALINE Model/Catalog Number: 91849 Product Description: NON-Sterile syringes without needles for single use Component: No
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V372000·2024-05-28
Mercedes EQ battery software can shut down causing sudden power loss
Mercedes-Benz is recalling certain 2023-2025 EQE and EQS models because battery management software may shut down the high-voltage battery, causing a sudden loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH EQS SUV 450 4MATIC, EQS SUV 450+, EQE SUV 350 4MATIC, EQE SUV 500 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V370000·2024-05-28
Forest River Recalls School Buses Due to Weak Roof Panel Joints
Forest River is recalling 854 school buses because the front roof panel may separate in a crash, increasing injury risk.
Product
STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER BUS QUEST, PRODIGY, STARCRAFT RONDAK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V376000·2024-05-28
Tesla seat belt warning light and chime may not activate
Tesla is recalling certain 2012-2024 vehicles because the seat belt warning light and audible chime may not activate for an unbelted driver, failing FMVSS 208. A free over-the-air update fixes it.
Product
TESLA — TESLA MODEL X, MODEL S, MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V374000·2024-05-28
BYD Recalls Transit Buses Due to Incorrect Fuse Fire Risk
BYD is recalling 2019-2023 transit buses because an incorrect fuse in the rearview mirror control switch may overheat and increase the risk of a fire.
Product
BYD — BYD K8M, K7M, C10M, K9S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V369000·2024-05-24
VinFast VF8 airbags may contain inactive ignitors preventing deployment
VinFast is recalling certain 2022-2024 VF8 vehicles because inactive ignitors may have been installed in the airbags, which can prevent them from deploying. 225 units affected.
Product
VINFAST — VINFAST VF 8
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V368000·2024-05-24
Lincoln Aviator rearview camera images may flicker near a cell phone
Ford is recalling certain 2020-2024 Lincoln Aviator vehicles because electromagnetic interference from a cell phone can cause the rearview camera image to flicker or distort.
Product
LINCOLN — LINCOLN AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V371000·2024-05-24
Mercedes-Benz Recalls 2023 AMG C43 Vehicles Due to Seat Wiring Defect
Mercedes-Benz is recalling 2023 AMG C43 vehicles because incorrectly routed seat wiring may damage the harness, preventing seat air bags from deploying in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG C43
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V363000·2024-05-23
KME Predator Fire Trucks Recalled for Parking Brake Defect
KME is recalling 2022-2023 Predator fire trucks because an incorrect relay valve may prevent the parking brake from engaging, allowing the vehicle to roll away.
Product
KME — KME redundant PREDATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V365000·2024-05-23
Blue Bird Recalls 2021-2023 Vision School Buses for Fuel Tank Leak
Blue Bird is recalling 2021-2023 Vision school buses because the diesel tank for the fuel-fired heater may leak fuel, creating fire and crash risks.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V362000·2024-05-23
Altec aerial device feeder tubes may leak and cause uncontrolled boom movement
Altec is recalling certain 2020-2024 LR7 and LR8 aerial devices because a hydraulic cylinder feeder tube may become damaged and leak oil, which can result in uncontrolled boom movement.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V364000·2024-05-23
Range Rover Sport rearview cameras may admit water and distort
Land Rover is recalling certain 2018-2022 Range Rover Sport vehicles with a Surround Camera System because water may enter the rearview camera, blanking or distorting the image.
Product
LAND ROVER — LAND ROVER RANGE ROVER SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V366000·2024-05-23
Chevrolet Colorado fitted with tires that do not match the label
GM is recalling certain 2024 Chevrolet Colorado vehicles because incorrect tires may have been installed that do not match the tire label, and the TPMS may report inaccurately.
Product
CHEVROLET — CHEVROLET COLORADO
Category
Vehicle
Distribution
Distributed nationwide