State

Missouri product recalls

20,324 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14026–14050 of 20324

HighFDA (Devices)·Z-1162-2023·2023-03-01
Medline Sterile Maximum Barrier Pack-LF units recalled for sterilization failure
Medline Industries recalls approximately 720 Sterile Maximum Barrier Pack-LF units due to improper component placement preventing sterilization. The affected packs were distributed in Arkansas, Colorado, and Georgia.
Product
(1) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546C, 6 kits per case, contains BD Chloraprep Hi-Lite Orange, 10.5 mL Applicator, Vendor PN: 930715NS; (2) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546D, 6 kits per case, contains BD Chloraprep Hi-Lite Oran
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1158-2023·2023-03-01
IV Access Device Kit Recalled Due to Manufacturing Defect in Connector
Cardinal Health is recalling Presource Packs IV START TRAY I kits due to a manufacturing defect in the ICU MicroClave Clear Connector that may cause fluid leaks and loss of fluid path integrity.
Product
Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0336-2023·2023-03-01
Levothyroxine Oral Solution TIROSINT Recalled Due to Subpotency
IBSA PHARMA is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency in specific batches. The affected product may contain less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0341-2023·2023-03-01
Thyroid Drug TIROSINT Recalled Due to Subpotent Formulation
IBSA Pharma Inc. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2023·2023-03-01
Hepatitis B Diagnostic Test Kits Recalled for Test Interference
Siemens is recalling ADVIA Centaur diagnostic test kits used to detect hepatitis B antibodies due to test interference that can produce false positive results when performed before another hepatitis B test on the same sample.
Product
ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- In vitro diagnostic immunoassay for the qualitative detection of antibodies to the e antigen of the hepatitis B virus (HBV) in human pediatric (2-21 years old) and adult serum, EDTA plasma, or lithium heparin. Siemens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0345-2023·2023-03-01
Prescription Levothyroxine Sodium Oral Solution Nationwide Recall Due to Subpotency
IBSA Pharma has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Affected lots 220418 and 220560 may contain insufficient active ingredient for proper thyroid hormone replacement therapy.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0346-2023·2023-03-01
FDA Recalls Sodium Chloride Injection Due to Incomplete Container Seals
B. Braun Medical's 0.9% Sodium Chloride Injection batches recalled due to risk of incomplete seals that could allow leakage, potentially compromising sterility. The recall affects 1,343,982 bags distributed nationwide.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2023·2023-03-01
HydroMID Peripheral Access Kit Recalled for Mislabeled Packaging
Access Vascular is recalling the HydroMID 4Fr Single Lumen Maximal Barrier Kit because the outer bag and inner Tyvek header bag are mislabeled. The device is used for short-term peripheral venous access.
Product
HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Model Number: 80004004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0340-2023·2023-03-01
FDA Recalls TIROSINT Levothyroxine Sodium Lot 220853 for Subpotency
IBSA Pharma Inc. recalled TIROSINT levothyroxine sodium lot 220853 nationwide due to subpotency. The oral solution may contain less active ingredient than labeled, potentially affecting thyroid hormone replacement therapy.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2023·2023-03-01
Diagnostic Imaging System Recalled for Potential Ceiling and Wall Collision Risk
Siemens Luminos dRF diagnostic imaging system is being recalled nationwide due to potential collision with ceilings, walls, or objects caused by default room configuration parameters. Collisions could result in serious injury to patients or staff.
Product
Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1167-2023·2023-03-01
Diagnostic imaging system recalled for collision risk from default settings
Siemens Luminos dRF Max diagnostic imaging systems are being recalled due to a risk of collision with ceiling, walls, or nearby objects caused by default room configuration settings. This could result in serious injury to staff or patients.
Product
Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762471
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0348-2023·2023-03-01
Warfarin Sodium Tablets Recalled Due to Failed Impurity and Degradation Specifications
Rising Pharmaceuticals is recalling Warfarin Sodium Tablets USP 1 mg due to failed impurities and degradation specifications. Approximately 12,216 bottles may have been distributed nationwide.
Product
Warfarin Sodium Tablets, USP 1 mg, 100-count bottle, Rx Only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC# 57237-119-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1156-2023·2023-03-01
HydroMID 4Fr Peripheral Venous Catheter Kit Recalled for Incorrect Component Labeling
Access Vascular is recalling HydroMID 4Fr Single Lumen Maximal Barrier Kits due to an incorrect component listed on the inner kit label. The error could lead to confusion and improper use of the device.
Product
HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Number: 80004004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1159-2023·2023-03-01
IV Start Kit Recalled Due to Connector Manufacturing Defect
Cardinal Health Presource Packs IV start kits with ICU MicroClave Clear Connectors are being recalled due to a manufacturing defect that may cause fluid leaks and loss of fluid path integrity.
Product
Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1168-2023·2023-03-01
Diagnostic imaging system recalled due to ceiling and wall collision risk
Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.
Product
Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0342-2023·2023-03-01
FDA Recalls TIROSINT Levothyroxine Sodium Oral Solution for Subpotency
IBSA Pharma Inc. voluntarily recalled specific lots of TIROSINT (levothyroxine sodium) Oral Solution nationwide due to subpotency. The affected medication contains less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1149-2023·2023-03-01
Siemens Atellica IM Folate 140 test kit recalled for measurement bias
Siemens is recalling the Atellica IM Folate 140 test kit due to negative bias that occurs when whole blood calibration is mistakenly used to test serum samples, potentially producing falsely low folate measurements.
Product
Atellica IM Folate 140 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10995572
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0334-2023·2023-03-01
Levothyroxine oral solution TIROSINT recalled nationwide for subpotency
IBSA Pharma voluntarily recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency concerns. Affected lots are 220416 (Exp. 10/2023) and 221053 (Exp. 4/2024).
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0330-2023·2023-03-01
Tacrolimus Capsules Recalled for Wrong-Strength Tablets Co-Mingled in Bottles
Dr. Reddy's Laboratories is recalling Tacrolimus 0.5 mg capsules due to the presence of one 1 mg capsule co-mingled in affected bottles. The mismatched capsule could lead to incorrect dosing in immunosuppressed patients.
Product
TACROLIMUS — TACROLIMUS (TACROLIMUS)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0338-2023·2023-03-01
Thyroid Medication TIROSINT Levothyroxine Sodium Nationwide Recall for Subpotency
IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. Two lot numbers are affected: Lot #220407 (Exp. 10/2023) and Lot #220960 (Exp. 03/2024).
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0337-2023·2023-03-01
TIROSINT Levothyroxine Sodium Oral Solution Recalled for Subpotency
TIROSINT (levothyroxine sodium) oral solution has been recalled nationwide by IBSA Pharma Inc. due to subpotency, with the affected medication containing less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2023·2023-03-01
Siemens Atellica IM Folate 700 test kit recalled for measurement bias
Siemens Healthcare is recalling 9,272 Atellica IM Folate 700 test kits due to negative bias in results when whole blood calibration is used to test serum samples.
Product
Atellica IM Folate 700 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10995573
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1165-2023·2023-03-01
Diagnostic imaging system recalled for collision risk from default settings
Siemens Luminos Agile Max diagnostic imaging systems recalled due to default configuration parameters allowing collision with room structures, risking serious injury to staff or patients.
Product
Luminos Agile Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10762472
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2023·2023-03-01
Atellica IM Folate test kit recalled for measurement bias issues
Siemens Healthcare is recalling 1,865 Atellica IM Folate 700 diagnostic kits nationwide and internationally. The kits may produce inaccurate folate test results when whole blood calibration is used instead of serum calibration.
Product
Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 11206252
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1157-2023·2023-03-01
IV START KIT Connector Defect May Cause Fluid Leaks
Cardinal Health's Presource Packs IV START KIT is being recalled due to a manufacturing defect in the connector that may cause fluid leaks and compromise intravenous fluid delivery.
Product
Cardinal Health Presource Packs IV START KIT- Intended for IV access device CATALOG #: 01-5798B
Category
Medical Device
Distribution
Distributed nationwide