State

Missouri product recalls

73,737 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,500
Critical: 1,339
Severe: 2,203
Most recent: 2026-10-28

Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31526–31550 of 82237

HighFDA (Devices)·Z-2267-2020·2020-06-17
Genicon GENILook Medical Device Recalled Due to Detachment Risk
Genicon, Inc. is recalling GENILook Model 200-005-152 medical devices because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-005-152, 5mm diameter, 100mm legnth (2 cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2343-2020·2020-06-17
RayStation 6 Service Pack 3 Radiation Therapy Software Recall
RaySearch Laboratories is recalling RayStation 6 Service Pack 3 software due to a calculation error that could underestimate radiation dose.
Product
RayStation 6 Service Pack 3, UDI # 07350002010242 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2020·2020-06-17
RayStation 7 Software Recalled for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 7 software due to errors in dose calculation algorithms that may underestimate radiation dose.
Product
RayStation 7, UDI # 07350002010068 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1290-2020·2020-06-17
Lupin Recalls Lisinopril 5 mg Tablets Due to Product Mix-Up
Lupin Pharmaceuticals is recalling 4,224 bottles of Lisinopril 5 mg tablets because 10 mg tablets were found in the bottles.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2278-2020·2020-06-17
Genicon GENILook Medical Device Recalled for Potential Tip Detachment
Genicon, Inc. is recalling GENILook Model 200-105-252 devices because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-105-252, 5mm diameter, 150mm length (2 cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighCPSC·20140·2020-06-17
Edwards Recalls Mechanical Heat Detectors Due to Fire Alert Failure
Edwards Fire Safety is recalling about 85,000 mechanical heat detectors that may fail to activate during a fire, posing a risk of failure to alert consumers.
Product
Edwards Mechanical Heat Detectors
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2283-2020·2020-06-17
Siemens Atellica CH Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Atellica CH Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
Atellica CH Enzymatic Creatinine_2, Siemens Material Number 11097533, UDI Number 00630414595795 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2020·2020-06-17
Philips Recalls IntelliSpace PACS 4.4 Due to Potential Image Corruption
Philips Healthcare Informatics is recalling 26 units of IntelliSpace PACS 4.4 because images may potentially become corrupt while using the system.
Product
IntelliSpace PACS 4.4, Product number 837507 - Product Usage: intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2270-2020·2020-06-17
Genicon GENILook Cannula Recalled Due to Potential Tip Detachment
Genicon, Inc. is recalling GENILook Model 200-105-151 cannulas because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-105-151, 5mm diameter, 100mm length (one cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighCPSC·20139·2020-06-17
Republic Wireless Recalls Relay Charging Cables Due to Overheating and Burn Hazards
Republic Wireless is recalling approximately 15,000 Relay charging cables sold between May 2018 and May 2019 because they can overheat and partially melt, posing a burn hazard.
Product
Charging Cable for Relay Screenless Communication Devices
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2282-2020·2020-06-17
Siemens ADVIA Chemistry Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens is recalling ADVIA Chemistry Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
ADVIA Chemistry Enzymatic Creatinine_2, Siemens Material Number 10335869, UDI Number 00630414526690 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2020·2020-06-17
RayStation 9B Software Recall for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 9B Service Pack 1 due to a software error in dose calculation algorithms that could result in local underestimation of expected radiation dose.
Product
RayStation 9B Service Pack 1, UDI # 07350002010297 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2020·2020-06-17
Inari Medical Recalls Triever20 Aspiration Guide Catheter for Valve Failure
Inari Medical is recalling 318 Triever20 Aspiration Guide Catheters because the hemostasis valve may fail to seal, causing loss of vacuum during thrombus aspiration.
Product
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-2345-2020·2020-06-17
RayStation 8A Software Recall for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 8A Service Pack 1 software due to a dose calculation error that could underestimate radiation therapy doses.
Product
RayStation 8A Service Pack 1, UDI # 07350002010136 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2354-2020·2020-06-17
Acuity A Link Z Spinal Fusion Device Recalled for Manufacturing Defect
Acuity Surgical Devices is recalling 178 A Link Z intervertebral body fusion devices because a manufacturing issue prevented bone screws from seating properly.
Product
A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Plate-Cage 32x21x15 7 A Link Z Ti Unitary Plate-Cage 32x21x15 12 A Link Z Ti Unitary Plate-Cage 32x21x15 16 A Link Z Ti Unitary Plate-Cage 32x21x15 16 A Link Z Ti Unitary Plate-Cage…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2020·2020-06-17
RayStation 6 Service Pack 1 Radiation Therapy Software Recall
RaySearch Laboratories is recalling RayStation 6 Service Pack 1 software due to a calculation error that may underestimate radiation dose.
Product
RayStation 6 Service Pack 1, UDI #s 07350002010037, 07350002010082 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2265-2020·2020-06-17
ROi CPS Recalls Custom Procedure Kits Containing Recalled BD Syringes
ROi CPS LLC is recalling 40 custom procedure kits because they contain PosiFlush Syringes from a lot previously recalled by BD.
Product
Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2020·2020-06-17
RayStation 9B Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 9B software due to a dose calculation error that could underestimate radiation therapy doses.
Product
RayStation 9B, UDI # 07350002010266 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2262-2020·2020-06-17
Ventana HE 600 Recalled for Electrical Short Risk
Ventana Medical Systems is recalling 461 HE 600 instruments due to a cleaning solution leak that can cause electrical shorts and burned components.
Product
Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System s intended use environment includes anatomic pathology (AP) laboratories and histology facilities within hospital, clinic, reference, or private lab settings. The System is to be operated by qualified…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2020·2020-06-17
BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results
BioFire Diagnostics is recalling FilmArray BCID Panels due to a risk of false positive Proteus results when used with specific blood culture media, which may lead to improper antibiotic treatment.
Product
FilmArray BCID Panel, RFIT-ASY-0127, 6, Rx Only, CE, IVD, UDI: 00815381020093 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT¿ FA Plus 410852/BACT/ALERT¿ FN Plus 410853/BACT/ALERT¿ PF Plus 259790/BACT/ALERT¿ SN…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2355-2020·2020-06-17
Acuity Surgical Devices Recalls A Link Z Intervertebral Body Fusion Devices
Acuity Surgical Devices is recalling A Link Z Intervertebral Body Fusion Devices due to a manufacturing issue that may prevent vertebral body bone screws from seating properly.
Product
A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbody 32x24x12 7 A Link Z Ti Unitary Open Interbody 32x24x12 12 A Link Z Ti Unitary Open Interbody 32x24x16 7 A Link Z Ti Unitary Open Interbody 32x24x16 12 Product Usage: is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2020·2020-06-17
HardyCHROM MRSA Recall for False Positive Results
Hardy Diagnostics is recalling HardyCHROM MRSA kits because they may produce false positive results for methicillin-susceptible Staphylococcus aureus.
Product
HardyCHROM MRSA,REF; G307, LOT: 447694, A selective and differential chromogenic medium for the qualitative direct detection of nasal colonization by methicillin-resistant Staphylococcus aureus (MRSA). Not intended to diagnose infection of guide therapy. Further testing required…
Category
Medical Device
Distribution
15 states
HighFDA (Food)·F-0982-2020·2020-06-17
ConAgra Recalls Healthy Choice Pesto and Egg Bowls Due to Stone Risk
ConAgra Foods is recalling Healthy Choice Pesto and Egg bowls because the farro ingredient may contain small stones.
Product
Healthy Choice Pesto and Egg bowls labeled in the following ways: 1) (for the US market) Healthy Choice Power Bowls Morning Pesto & Egg White Scramble, Net Wt. 7.2 OZ (204 g); UPC 0-72655-00083-4 2) (for the Canadian market) Healthy Choice, Power Bowls, All-Day Breakfast, Pesto…
Category
Food
Distribution
19 states
HighFDA (Drugs)·D-1306-2020·2020-06-17
Pfizer Recalls Unasyn Injection Due to Particulate Matter
Pfizer is recalling specific lots of Unasyn (ampicillin sodium and sulbactam sodium) for injection because particulate matter was identified after reconstitution.
Product
UNASYN — UNASYN (AMPICILLIN SODIUM AND SULBACTAM SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2284-2020·2020-06-17
Siemens Dimension Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Dimension Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
Dimension Enzymatic Creatinine, Siemens Material Number 10471520, UDI Number 00842768030512 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide