State

Missouri product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10776–10800 of 81589

SevereFDA (Devices)·Z-2444-2024·2024-08-14
Medline Procedure Kits Recalled Due to Defective Syringes and Quality Issues
Medline procedure kits containing defective plastic syringes have been recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects over 1.6 million units distributed worldwide.
Product
Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ5
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1691-2024·2024-08-14
Wiers Farm Mixed Vegetables Recalled for Listeria Contamination
Wiers Farm is recalling approximately 1,720 cases of mixed vegetables due to potential Listeria monocytogenes contamination. Affected lot numbers 240705-240712 were distributed across 17 states.
Product
Wiers Farm - Mixed Vegetable box packaged in cartons - carton size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1679-2024·2024-08-14
Wiers Farm Green Beans Recalled for Listeria monocytogenes Contamination
Wiers Farm is recalling green beans due to potential Listeria monocytogenes contamination. The recall affects 3,274 cases distributed across 16 states.
Product
Wiers Farm - Green Beans packaged in varied weighted bags
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1697-2024·2024-08-14
Wiers Farm Butternut Squash Recalled for Listeria Monocytogenes
Wiers Farm Inc is recalling Butternut Squash in 1-pound cartons due to potential Listeria monocytogenes contamination. Lot numbers 240705 through 240712 are affected.
Product
Wiers Farm - Butternut Squash packaged in 1lb cartons - case size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1660-2024·2024-08-14
Patriotic Pretzel Products Recalled for Potential Salmonella Contamination
Palmer & Company is recalling Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists and Palmer Candy Frosted Patriotic Pretzels nationwide due to potential salmonella contamination.
Product
1. Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists, Net Wt 14 oz., UPC 78742 03913, 8/14oz case 2. Palmer Candy Frosted Patriotic Pretzels, Item 10757, Net Wt 28 lbs, UPC 77232 10757
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1665-2024·2024-08-14
Palmer Candy Munchy Medley products recalled due to potential salmonella contamination
Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.
Product
1. Palmer Candy Munchy Medley, Item 38004, Net Wt. 16/6oz bulk case, UPC 77232 38004 2. Palmer Candy Munch Medley, Item 10737, Net Wt. 15 lbs, UPC 77232 10737 3. Casey's Munchy Medley, Sweet & Salty Crunch Mix, Net Wt. 4.25 oz, UPC 98437 26083 6/case 4. Snackin' with the Crew! Mi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1685-2024·2024-08-14
Wiers Farm Jalapenos Recalled for Potential Listeria Contamination
Wiers Farm jalapenos in 8oz bags are being recalled due to potential Listeria monocytogenes contamination. The recall affects 5,331 cases distributed across 16 states.
Product
Wiers Farm - Jalapenos packaged into 8oz bags - case size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1689-2024·2024-08-14
Green Bell Peppers Recalled for Listeria monocytogenes Contamination
Wiers Farm green bell peppers packaged in 1-pound cartons are being recalled due to potential Listeria monocytogenes contamination. Affected lot numbers are 240705 through 240712, distributed across 17 states.
Product
Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2489-2024·2024-08-14
BD PYXIS MEDBANK Automated Cabinet May Print Incorrect Medication Bin Labels
A software issue in the BD PYXIS MEDBANK automated medication dispensing cabinet can cause incorrect bin labels to be printed for restock operations. This could lead to medication administration errors affecting patient safety.
Product
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2499-2024·2024-08-14
Automated Medication Dispenser Software Bug Causes Incorrect Bin Labels
BD PYXIS MEDBANK automated medication dispensers may print incorrect medication bin labels due to a software defect, risking medication handling errors in healthcare settings.
Product
BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2512-2024·2024-08-14
Baxter Precision Surgical Table Recall: Loose Spring Pins Risk
Baxter Healthcare Corporation is recalling the PST 500 U Precision Surgical Table due to loose spring pins that can cause the tabletop to unexpectedly tilt or move, potentially causing unintended patient movement during surgery.
Product
Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2518-2024·2024-08-14
Gyn Laparoscopy Kits Recalled Due to Inadequate Sterilization Process
American Contract Systems is recalling 29 gynecological laparoscopy surgical kits due to insufficient aeration during sterilization, which may compromise sterility and increase infection risk for patients.
Product
American Contract Systems Gyn Laparoscopy convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2502-2024·2024-08-14
Automated Dispensing Cabinet Software Issue Causing Incorrect Medication Bin Labels
A software defect in the BD PYXIS MEDBANK automated dispensing cabinet causes incorrect medication bin locations to be printed on restock labels, potentially resulting in medication dispensing errors. No illnesses or injuries have been reported.
Product
BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2534-2024·2024-08-14
Philips Azurion X-ray System: Potential Loss of Imaging Functionality
The Philips Azurion Interventional Fluoroscopic X-ray System may lose imaging functionality or experience longer restart times. The FDA is recalling approximately 3,011 units of this device worldwide.
Product
Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for Image guidance in diagnostic, interventional, and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, car
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2519-2024·2024-08-14
American Contract Systems surgical kits recalled for sterilization defect
American Contract Systems Laparoscopy and Lap Chole surgical kits are being recalled because insufficient aeration time after sterilization may have compromised their sterility. The kits were distributed in seven U.S. states.
Product
American Contract Systems Laparoscopy Litho Std Pack convenience kit and American Contract Systems Lap Chole convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0630-2024·2024-08-14
Estradiol Cypionate Injection Recalled Due to Lack of Sterility Assurance
Empower Pharmacy is recalling Estradiol Cypionate Injection due to lack of assurance of sterility. The recall affects 2,797 units distributed nationwide within the United States.
Product
Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2532-2024·2024-08-14
FDA Recalls CryoPatch Cardiac Tissue Grafts Due to Invalid Test Results
Artivion has recalled CryoPatch SG cardiac tissue patches used in pulmonary surgeries due to approval and release with invalid test results. Patients who received implants should consult their healthcare provider.
Product
(1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2490-2024·2024-08-14
BD PYXIS automated medication cabinet software defect causes incorrect bin labels
A software defect in BD PYXIS MEDBANK automated medication dispensing cabinets may cause the incorrect medication bin to be printed on restock labels, potentially resulting in medication errors.
Product
BD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2523-2024·2024-08-14
Biopsy Drape Pack sterilization failure recall from American Contract Systems
American Contract Systems is recalling 224 Biopsy Drape Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised the sterility of affected units. Lot 981241 distributed in CA, KS, ME, MN, MO, NE, and SD is affected.
Product
American Contract Systems Biopsy Drape Pack convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2525-2024·2024-08-14
Siemens x-ray display system support arm may lower unexpectedly
Siemens Luminos Agile Max x-ray imaging systems have a support arm that may unintentionally lower during display positioning, creating an injury risk.
Product
Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2537-2024·2024-08-14
Medical Device Hookup Instructions Incorrect, Risking Endoscope Disinfection
Steris Corporation recalls 129 Hookup devices (Model 2-8-540HAN) due to incorrect hookup instructions in product documentation. Using wrong connections may prevent proper endoscope disinfection, creating infection risk.
Product
Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Thru Automated Endoscope Reprocessor ( AER ) and endoscopes, which allow perfusion of liquids dispens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2531-2024·2024-08-14
Pulmonary Heart Valve Grafts Recalled Due to Invalid Test Results
Artivion is recalling two CryoValve SG heart valve grafts that were approved and implanted with invalid test results.
Product
CryoValve SG Pulmonary Human Heart Valve, SGPV00, Cryopreserved Decellularized Heart Valve Allograft Prepared with SynerGraft (SG) Technology.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2542-2024·2024-08-14
Olympus Everest Bipolar Cutting Forceps Recalled for Packaging Defects
Olympus is recalling Everest Bipolar Cutting Forceps due to fractures and breakages in packaging trays and Tyvek covers that may compromise sterility. The recall affects 4,364 units distributed worldwide.
Product
The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgical energy under visualization. The device is to be used with bipolar outputs of c
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2485-2024·2024-08-14
Automated medication cabinet software prints incorrect bin labels
The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.
Product
BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2529-2024·2024-08-14
Paraffin Embedding Station Recalled for Internal Fire and Toxic Smoke Risk
The FDA is recalling 180 Leica HistoCore Arcadia H paraffin embedding stations due to a sealing defect in the paraffin tank that can cause toxic smoke and internal fire.
Product
Leica HistoCore Arcadia H, REF: 14039354100 and 14039357258, Paraffin Embedding Station.
Category
Medical Device
Distribution
Distributed nationwide