State

Missouri product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6301–6325 of 81434

SevereFDA (Drugs)·D-0506-2025·2025-07-09
Orajel Baby teething swabs recalled over fungal contamination of swabs
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
Product
Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0499-2025·2025-07-09
Bupivacaine HCL Sterile Injection Recalled for Sterility Assurance Concerns
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Product
BUPIVAcaine HCL Sterile injection, USP w/EPINEPHRINE 1:200,000, 50 mg/10mL, 0.5%, (5mg/mL), 10 mL Sterile Single-Dose Vial, Rx Only, For Nerve Block, Caudal & Epidural Anesthesia Only, Warning: Contains Sulfites, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0570-2025·2025-07-09
Buffered penicillin G potassium vials may actually contain cefazolin for injection
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
Product
PENICILLIN G POTASSIUM — PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2014-2025·2025-07-09
Servo-n ventilators may measure patient circuit compliance inaccurately
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Product
Servo-n Ventilator System. Model Number: 6694800.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2036-2025·2025-07-09
BiPAP A30 and BiPAP Hybrid A30 Ventilators Recalled by Philips
Philips Respironics is recalling BiPAP A30 and BiPAP Hybrid A30 ventilators. The devices do not have an indication for use in patients with respiratory failure.
Product
BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2048-2025·2025-07-09
Philips Ultrasound Transducers Recalled After Over-Refurbishment
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Product
Philips 3D9-3v Transducer.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2035-2025·2025-07-09
BiPAP V30 Auto ventilators are not indicated for respiratory failure
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Product
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2041-2025·2025-07-09
HardyCHROM CRE Culture Medium Recalled for Quality Control Failure
Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.
Product
HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No. G323
Category
Medical Device
Distribution
22 states
SevereFDA (Drugs)·D-0503-2025·2025-07-09
Lidocaine HCL Sterile Injection recalled for sterility assurance concerns
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Product
LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2015-2025·2025-07-09
Servo-u MR Ventilator System inaccurate patient circuit compliance measurement
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Product
Servo-u MR Ventilator System. Model Number: 6888800.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0504-2025·2025-07-09
Zicam cold remedy nasal swabs recalled over fungal contamination
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
Product
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2069-2025·2025-07-09
Apex Knee System components recalled over loss of sterile packaging integrity
Apex Knee System components are being recalled because the age of the nylon packaging material has caused a loss of integrity of some pouches. 341 units are affected.
Product
Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0501-2025·2025-07-09
Compounded ketamine multi-dose vials recalled over sterility assurance concerns
Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.
Product
KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0212-2025·2025-07-09
Vita Warehouse Vitamin B12 Gummies Recalled for Undeclared Peanut
Vita Warehouse Corp. is recalling four Vitamin B12 gummy products nationwide due to undeclared peanut allergen. Consumers with peanut allergies should not use the affected products.
Product
1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0203-2025·2025-07-09
Peak Cocktails blood orange spritz cans may overpressurize and explode
Peak Cocktails Blood Orange Spritz in 8.4 fl oz cans is being recalled because of overpressurization leading to exploding cans. 16,128 units are affected.
Product
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-2074-2025·2025-07-09
BD Heyman Follower Straight Tip catheters with incorrect French size packaging
C.R. Bard Inc is recalling BD Heyman Follower Straight Tip catheters because packaging may contain an incorrect French size designation, which could lead to use of the wrong catheter size.
Product
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V461000·2025-07-09
Prevost Recalls 2018-2019 X3-45 Commuters for Incorrect Window Glazing
Prevost is recalling 2018-2019 X3-45 Commuter vehicles because incorrect entrance door window glazing may reduce driver visibility and increase crash risk.
Product
PREVOST — PREVOST X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2072-2025·2025-07-09
Cardiology hemodynamics software update may cause unexpected system shutdowns
Change Healthcare Cardiology Hemodynamics Software version 15.0.1 is being recalled because, following complaints, a software update may cause the software to unexpectedly shut down.
Product
Change Healthcare Cardiology Hemodynamics Software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2025·2025-07-09
Philips S5-1 Ultrasound Transducers Refurbished Beyond Useful Life
Philips Ultrasound is recalling Philips S5-1 Transducers because they were refurbished beyond their useful life, which may affect device performance and safety.
Product
Philips S5-1 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2025·2025-07-09
ADVIA Hematology System Control Product Recall for Platelet Value Error
Siemens Healthcare Diagnostics is recalling 3,266 units of ADVIA 120/2120/2120i 3-in-1 TESTpoint Control worldwide due to incorrect platelet value assignments that could affect test results.
Product
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0498-2025·2025-07-09
Compounded preservative-free lidocaine vials lack assurance of sterility
Preservative-free Lidocaine HCl Injection 1%, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 29,700 vials are affected.
Product
LIDOcaine HCl Injection, USP, 10mg/mL, 1% (100 mg/10mL), 10 mL Sterile Single Dose Vial, Rx Only, For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative-Free, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S Kyrene Rd., Chandler, AZ, 8522
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2025·2025-07-09
Bard Urologist's Tray Recalled Over Incorrect French Size Labeling
C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0500-2025·2025-07-09
Compounded ketamine injection recalled over lack of sterility assurance concerns
Ketamine Hydrochloride Injection compounded by Medivant Healthcare is being recalled for lack of assurance of sterility after an FDA inspection raised concerns about the sterile manufacturing process.
Product
KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler, AZ 85226, NDC 81483-0006-0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2044-2025·2025-07-09
Medline IV Catheter Kits Recalled Over Needle Retraction Issue
Medline is recalling 36 Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN due to a potential needle retraction failure during insertion.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2043-2025·2025-07-09
Medline IV Catheters Recalled for Needle Retraction Failure
Medline Industries is recalling specific Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters because the needle may be slow to retract or fail to retract during catheter insertion.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
Category
Medical Device
Distribution
Distributed nationwide