State

Missouri product recalls

73,376 recalls have nationwide distribution and so reach Missouri. 8,494 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,494
Critical: 1,344
Severe: 2,198
Most recent: 2026-10-07

Of the 8,494 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 2,198 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,494 recalls whose distribution notice names Missouri specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19851–19875 of 81870

HighFDA (Devices)·Z-0278-2023·2022-11-30
PAJUNK Continuous Epidural Tray Recalled for Wrong Medication in Kit
Pajunk Medical Systems is recalling PAJUNK Continuous Epidural Trays (Model TAL101, Lot 0001359) because some contain 0.75% Marcaine Spinal instead of the intended 0.9% Sodium Chloride. This medication substitution could lead to improper drug administration during epidural procedures.
Product
PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model #TAL101, sterile, each tray contains 5ml Ampule 1% Lidocaine HCl, 10ml Ampule 0.9% Sodium Chloride, and 5ml Ampule 1.5% Lidocaine HCl with Epinephrine 1:200,000.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0282-2023·2022-11-30
VS3 Iridium Visionsense Beam Combiner Optical Fiber Cable Damage Risk
Visionsense VS3 Iridium beam combiners may develop damaged optical fiber cables through handling or bending, causing loss of functionality and potential cable heating or melting. Affected units were distributed nationwide in the US.
Product
VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0283-2023·2022-11-30
Regard LAMINECTOMY surgical kits recalled due to recalled 3M drapes
ROi CPS LLC is recalling Regard LAMINECTOMY surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled.
Product
regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Food)·F-0166-2023·2022-11-30
G FUEL Watermelon Limeade Energy Drink recalled for incorrect caffeine labeling
G FUEL LLC is recalling 48,000 units of GFUEL brand Watermelon Limeade Energy Drink nationwide because the product label does not declare the correct amount of caffeine.
Product
GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; ready-to-drink energy beverage in a can
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0311-2023·2022-11-30
Neuro surgery kits recalled for defective 3M surgical drapes
ROi CPS LLC is recalling 790 neuro surgery convenience kits that contained 3M surgical drapes which were subsequently recalled. The kits were distributed to Louisiana, Missouri, North Carolina, and Florida.
Product
regard MINOR NEURO, NU00140AD, Item Number 880135030; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0294-2023·2022-11-30
Surgical Convenience Kits Recalled for Containing Recalled 3M Surgical Drapes
ROi CPS LLC is recalling 170 surgical convenience kits containing 3M surgical drapes that were previously recalled. The kits were distributed to medical facilities in Louisiana, Missouri, North Carolina, and Florida.
Product
regard SHOULDER W BCH CHAIR, OR00356F, Item Number 800203006; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0293-2023·2022-11-30
Surgical convenience kits recalled due to defective surgical drapes
Regard MAJOR EAR surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida are being recalled because the kits contained 3M surgical drapes that were subsequently recalled.
Product
regard MAJOR EAR, ET00326J, Item Number 800070010; ear surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0301-2023·2022-11-30
Surgical kits recalled: Regard VITRECTOMY PK contained 3M recalled components
Regard VITRECTOMY PK surgical convenience kits are being recalled because they contain 3M surgical drapes that were separately recalled. Affected kits were distributed in Louisiana, Missouri, North Carolina, and Florida.
Product
regard VITRECTOMY PK, EY00938C, Item Number 800733003; EYE surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0274-2023·2022-11-30
Basin Set Medical Device Kit Contents Do Not Match Label
American Contract Systems, Inc. is recalling a surgical basin set (MEBS42K) because the kit contents do not match the labeled contents. The mismatch could result in improper surgical preparation.
Product
BASIN SET, MEBS42K, general surgical kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0319-2023·2022-11-30
Surgical Convenience Kits Recalled Due to Included 3M Surgical Drapes
ROi CPS LLC is recalling 54 regard LATERAL SHOULDER surgical convenience kits containing 3M surgical drapes that were subsequently recalled by the manufacturer. Affected kits were distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.
Product
regard LATERAL SHOULDER, OR01044C, Item Number 880435003; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0321-2023·2022-11-30
Regard SPINE Surgical Kits Recalled for Containing Unsafe Drapes
ROi CPS LLC is recalling 302 Regard SPINE surgical convenience kits containing 3M surgical drapes that were subject to an FDA recall. Affected kits were distributed in Louisiana, Missouri, North Carolina, and Florida.
Product
regard SPINE, OR01100A, Item Number 880468001; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0312-2023·2022-11-30
Neurosurgery convenience kits recalled due to included recalled surgical drapes
ROi CPS LLC is recalling 248 regard NEURO TRAY neurosurgery convenience kits because they contain 3M surgical drapes that were previously recalled. The kits were distributed in LA, MO, NC, and FL.
Product
regard NEURO TRAY, NU00160R, Item Number 880158018; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0300-2023·2022-11-30
Regard Retinal Pack surgical kits recalled for defective 3M drapes
ROi CPS LLC is recalling Regard Retinal Pack surgical kits distributed in Louisiana, Missouri, North Carolina, and Florida because they contained recalled 3M surgical drapes.
Product
regard RETINAL PACK, EY00935C, Item Number 800730003; EYE surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0304-2023·2022-11-30
Hip Arthroplasty Surgical Convenience Kits Recalled Due to Defective 3M Drapes
ROi CPS LLC is recalling regard TOTAL HIP ARTHROPLASTY surgical convenience kits containing recalled 3M surgical drapes distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.
Product
regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0292-2023·2022-11-30
Neurosurgery Kits Recalled Due to Defective 3M Surgical Drapes
ROi CPS LLC is recalling 38 neurosurgery convenience kits distributed in four states because they contain 3M surgical drapes that were separately recalled.
Product
regard CERVICAL PACK, NU00303H, Item Number 800058008; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0280-2023·2022-11-30
Visionsense Infrared Microscope Recalled Due to Optical Fiber Cable Damage
Visionsense is recalling 205 units of its VS3 Iridium microscope because optical fiber cables may become damaged during handling, causing loss of function and outer cable heating or melting.
Product
VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0279-2023·2022-11-30
Surgical Blade Safety Cartridges Recalled Due to Missing Sterilization
Southmedic is recalling 450 units of sterile surgical blade cartridges (Lot W92761) because the product was not sterilized but was labeled and distributed as sterile. Non-sterile surgical blades could cause infection if used on patients.
Product
Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0288-2023·2022-11-30
Surgical Convenience Kits Recalled Due to Defective 3M Surgical Drapes
ROi CPS LLC is recalling regard BASIC NEURO surgical convenience kits containing 3M surgical drapes that were previously recalled. Affected units were distributed to LA, MO, NC, and FL.
Product
regard BASIC NEURO, NU00259S, Item Number 800021019; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0308-2023·2022-11-30
Surgical convenience kits recalled for defective 3M drape components
ROi CPS LLC recalls 213 surgical convenience kits containing 3M surgical drapes that were subsequently recalled. The affected kits were distributed in Louisiana, Missouri, North Carolina, and Florida.
Product
¿regard SHOULDER PK, GS00125U, Item Number 880120021; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0302-2023·2022-11-30
Surgical Convenience Kits with Recalled 3M Surgical Drapes
ROi CPS LLC is recalling 21 surgical convenience kits distributed to Louisiana, Missouri, North Carolina, and Florida because they contain 3M surgical drapes that were subsequently recalled.
Product
regard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0265-2023·2022-11-30
B. Braun Central Venous Catheter Tray Recalled for Incorrect Expiration Date Label
Medical Action Industries is recalling 240 cases of B. Braun CARESITE Port Access Kits (REF 375214) due to incorrect expiration date labeling. The kits show an expiration date of 02/21/2024 when the actual expiration is 02/10/2024.
Product
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0298-2023·2022-11-30
Surgical Convenience Kits Recalled Due to Recalled Surgical Drapes
Regard ACDF surgical convenience kits containing 3M surgical drapes that were subsequently recalled are being recalled by ROi CPS LLC. Approximately 30 kits were distributed in Louisiana, Missouri, North Carolina, and Florida.
Product
regard ACDF, NU00698I, Item Number 800246009; neuro surgery convenience kit
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0291-2023·2022-11-30
Surgical convenience kits recalled due to included recalled 3M drapes
Surgical convenience kits (regard NEURO PACK) were recalled because they contain 3M surgical drapes that are subject to a separate recall. Affected units were distributed to healthcare facilities in Louisiana, Missouri, North Carolina, and Florida.
Product
regard NEURO PACK, NU00278L, Item Number 800040012; nuero surgery convenience kit
Category
Medical Device
Distribution
4 states
HighNHTSA·22V885000·2022-11-30
Mazda Recalls 2020-2021 Mazda2 Vehicles for Missing Headlight Caps
Mazda is recalling 2020-2021 Mazda2 vehicles because missing headlight adjustment caps allow improper alignment, increasing crash risk.
Product
MAZDA — MAZDA MAZDA2
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0305-2023·2022-11-30
Surgical Convenience Kits Recalled by ROi CPS Due to Included 3M Surgical Drapes
ROi CPS LLC is recalling 456 surgical convenience kits containing 3M surgical drapes that were subject to a separate recall. The kits were distributed across Louisiana, Missouri, North Carolina, and Florida.
Product
¿regard SHOULDER ARTHROSCOPY, OR00049Q, Item Number 880044017; ortho surgery convenience kit
Category
Medical Device
Distribution
4 states