State

Missouri product recalls

72,992 recalls have nationwide distribution and so reach Missouri. 8,465 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,465
Critical: 1,334
Severe: 1,870
Most recent: 2026-09-16

Of the 8,465 recalls naming Missouri we have scored against our rubric, 1,334 (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 8,465 recalls whose distribution notice names Missouri specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8376–8400 of 81457

SevereFDA (Devices)·Z-0824-2025·2025-01-22
ESSENTIO DR Pacemakers May Malfunction Due to Battery Impedance Issue
Boston Scientific is recalling certain ESSENTIO DR Pacemakers manufactured before September 2018 due to latent battery impedance that may cause Safety Mode malfunction during normal operations.
Product
ESSENTIO DR Pacemaker, SL (Model Number L101, SL MRI (Model Number L111), EL (Model Number L121), and EL MRI (Model Number L131)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0827-2025·2025-01-22
VISIONIST CRT-P Pacemakers Recalled Due to Battery Impedance Risk
Certain VISIONIST CRT-P pacemakers with latent high battery impedance may initiate Safety Mode unexpectedly during normal operations. Manufactured before September 2018, 156,329 units were distributed worldwide.
Product
VISIONIST CRT-P, EL (Model Number U225 and U226) and EL MRI (Model Number U228)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0826-2025·2025-01-22
CRT-P Pacemakers Recalled for Potential Safety Mode Initiation Risk
Boston Scientific's ACCOLADE Family pacemakers, including VALITUDE CRT-P models, are recalled due to battery impedance defects that could trigger unintended Safety Mode during normal operation.
Product
VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0831-2025·2025-01-22
Dialysis Blood Circuit May Cause Excessive Fluid Removal
The AquaFlexFlow UF 500 Plus blood circuit may malfunction and remove excessive fluid from patients, causing a dangerous drop in blood volume. This risk is especially dangerous for pediatric patients.
Product
nuwellis AquaFlexFlow UF 500 Plus, REF 114156, Catalog Number A06163, extracorporeal blood circuit which is used with the Aquadex SmartFlow or Aquadex FlexFlow System
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0885-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger May Cause Device Inoperability
Baxter Healthcare is recalling 946 Welch Allyn Life2000 ventilators due to a battery charger defect that can trigger an alarm and render the device inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0829-2025·2025-01-22
Impella RP Heart Pump Recalled Due to Optical Sensor Damage Risk
Abiomed is recalling 1,560 units of the Impella RP with SmartAssist pump due to risk of optical sensor damage from device interactions. Damaged sensors may cause temporary or permanent pump malfunction.
Product
Impella RP with SmartAssist; Product Number: 0046-0035;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0837-2025·2025-01-22
Karl Storz Biopsy and Grasping Forceps Recalled Due to Sterility Validation Failure
Karl Storz Endoscopy is recalling 285 units of optical biopsy and grasping forceps (REF 723400) distributed across 31 US states due to failure of manual cleaning validation, which compromises sterility assurance.
Product
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Category
Medical Device
Distribution
32 states
HighFDA (Devices)·Z-0902-2025·2025-01-22
VITROS DGXN Slides Recalled Due to Hemoglobin Interference in Digoxin Measurement
VITROS DGXN Slides are recalled because hemoglobin can interfere with digoxin measurement, producing artificially low results. Approximately 1,541 units were distributed in the US and internationally.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products DGXN Slides Model/Catalog Number: 8343386 Software Version: Not Applicable Product Description: The VITROS DGXN Slide is a multilayered, analytical element coated on a polyester support. Digoxi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0864-2025·2025-01-22
8MM Large Suturecut Needle Driver Recalled for Frayed Grip Cables
Intuitive Surgical is recalling 8MM Large Suturecut Needle Driver instruments due to frayed or broken grip cables. The recall affects 784 units distributed nationwide and internationally.
Product
8MM,LARGE SUTURECUT NEEDLE DRIVER,IS4000¿ REF 470296
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0943-2025·2025-01-22
ECONO STERILE medical procedure kits recalled for potential sterile barrier breach
Sklar Instruments is recalling three models of ECONO STERILE medical procedure kits nationwide due to packaging issues that may breach the sterile barrier. No injuries or illnesses have been reported.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE SIMS UTERINE CURETTE #3 STER25, Model Number 96-4113; 2) ECONO STERILE KEVORK ENDO CURET W/BAS STER25, Model Number 96-4144A; 3) ECONO STERILE KEVORKIAN CURET W/O BAS STER25, Model Number 96-4145A; cervical
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0961-2025·2025-01-22
VerifyNow P2Y12 Platelet Reactivity Test distributed without FDA market clearance
Accriva Diagnostics distributed the VerifyNow P2Y12 Platelet Reactivity Test (Lot WL1145) without required FDA clearance. Healthcare professionals could use the unapproved test to guide treatment decisions for P2Y12 inhibitor therapy.
Product
VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0397-2025·2025-01-22
Yu Yee Five Spice Powder Recalled for High Lead Levels
Summit Import Corporation is recalling Yu Yee Five Spice Powder due to high levels of lead detected in testing. Consumers should discontinue use and contact a healthcare provider with concerns.
Product
Yu Yee, Five Spice Powder,1.76oz
Category
Food
Distribution
15 states
HighFDA (Devices)·Z-0928-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Gynecological Procedure Kits for Packaging Defects
Sklar Instruments is recalling ECONO STERILE gynecological procedure kits (Model 96-2478) due to packaging issues that may breach the sterile barrier and create contamination risk.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SIMS UTERINE SND GRD 13"STER25, Model Numbers: 96-2478 (gynecological use)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0956-2025·2025-01-22
Murata Vios Cardiac Monitor Model 2050 Displays Distorted and Flickering Waveforms
The muRata Vios Monitoring System Model 2050 central station monitor can display distorted and flickering ECG waveforms and vital signs. The issue affects only the central station display, not the bedside monitor or patient monitoring accuracy.
Product
muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0949-2025·2025-01-22
Sklar Instruments ECONO STERILE surgical procedure kits recalled due to packaging defect
Sklar Instruments is recalling ECONO STERILE ALFONSO INFANT SPEC STRL sterile surgical procedure kits nationwide due to packaging issues that may breach the sterile barrier.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE ALFONSO INFANT SPEC STRL CS/10, Model Number 96-3814; eyelid surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0945-2025·2025-01-22
Gynecological Procedure Kits Recalled for Potential Sterile Barrier Packaging Defects
Sklar Instruments is recalling ECONO STERILE gynecological procedure kits due to packaging issues that may compromise the sterile barrier. The affected kits may no longer maintain their sterile condition.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE KOGAN ENDOCERV SPEC STER CS/5, Model Number 96-4142A, gynecological procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0918-2025·2025-01-22
Portrait Core Services Software Loss of Patient Monitoring After 425 Days
A software issue in GE's Portrait Core Services medical device software causes loss of patient monitoring capability in the Portrait Central Viewer Application after 425 days of continuous operation.
Product
Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile Monitoring Solution components and will integrate into existing healthcare facility infrastructure and clinical information systems, Model CSSXB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0927-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Trousseau Dilator Kits for Packaging Defects
Sklar Instruments is recalling ECONO STERILE trousseau dilator kits (Model 941-0191) distributed nationwide due to packaging issues that may compromise the sterile barrier. Affected healthcare providers should stop use immediately.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE TROUSSEAU DILATOR CS/25, Model Number 941-0191 (tracheal procedures)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0823-2025·2025-01-22
PROPONENT DR Pacemaker Recalled for Unexpected Safety Mode Risk
Boston Scientific is recalling certain PROPONENT DR pacemakers built before September 2018 due to latent battery impedance that could cause unexpected Safety Mode initiation during normal operation.
Product
PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221), and EL MRI (Model Number L231).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0835-2025·2025-01-22
Alcon Monarch III D Delivery Cartridge Recalled for Molding Defect Risk
Alcon is recalling 41,718 units of its Monarch III D Delivery Cartridge due to a molding defect that could scratch the intraocular lens during cataract surgery.
Product
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description: Monarch¿ III D delivery cartridge Lens Guide, Intraocular Component: N/A
Category
Medical Device
Distribution
51 states
HighFDA (Drugs)·D-0202-2025·2025-01-22
FDA recalls glipiZIDE Extended-Release Tablets for failed dissolution specifications
Amerisource Health Services LLC is recalling glipiZIDE Extended-Release Tablets, 2.5 mg, due to failed dissolution specifications. Patients should contact their pharmacist or healthcare provider.
Product
glipiZIDE, Extended-Release Tablets, 2.5 mg, 30-count (3x10 blister cards) carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC: 60687-480-21, Unit Dose NDC: 60687-480-11
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V027000·2025-01-22
Starcraft Bus Recalls 2023-2024 Models for Emergency Exit Handle Issues
Forest River is recalling 2023-2024 Starcraft Starlite and Allstar buses because emergency exit handles are not easily accessible, potentially delaying passenger evacuation.
Product
STARCRAFT BUS — STARCRAFT BUS ALLSTAR, STARLITE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0866-2025·2025-01-22
Surgical Retractor Instruments Recalled Due to Frayed or Broken Grip Cables
Intuitive Surgical is recalling approximately 9,303 units of 8MM Small Grasping Retractor instruments due to increased complaints of frayed or broken grip cables affecting reusable surgical instruments distributed nationwide and internationally.
Product
8MM,SMALL GRASPING RETRACTOR,IS4000¿ REF 470318
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0940-2025·2025-01-22
ECONO STERILE Procedure Kits Recalled for Sterile Barrier Breach Risk
Sklar Instruments is recalling ECONO STERILE medical procedure kits (Model 96-4921A) due to packaging issues that may result in a breach of the sterile barrier. The kits should not be used.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE BLAKE GALLSTONE FCP CVD 8"CS25, Model Number 96-4921A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0951-2025·2025-01-22
Sklar Instruments iris hooks recalled for sterile packaging integrity issues
Sklar Instruments is recalling ECONO STERILE iris hook surgical kits due to packaging defects that may compromise sterile barrier integrity. No injuries reported.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE IRIS HOOK QK REL 4MM 9" STER25, Model Number 96-2224A; eye surgery
Category
Medical Device
Distribution
Distributed nationwide