State

Missouri product recalls

73,088 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 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9226–9250 of 81581

SevereFDA (Devices)·Z-0375-2025·2024-11-27
Baxter peritoneal dialysis transfer set recalled for PCB exposure risk
Baxter MiniCap Extended Life PD Transfer Sets (Part 5C4482S) are being recalled due to potential exposure to polychlorinated biphenyls (PCBs). The FDA Class I recall affects 151,020 units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0377-2025·2024-11-27
Baxter Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare is recalling the MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Approximately 410,862 units are affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V897000·2024-11-27
Jeep Grand Cherokee side airbags may not deploy in a crash
Chrysler is recalling certain 2022-2024 Grand Cherokee and 2021-2024 Grand Cherokee L vehicles because an improperly secured connector may prevent the front seat side airbags deploying. All units have been remedied.
Product
JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V900000·2024-11-27
Honda Passport and Pilot fuel filler pipes can separate and leak
Honda is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles because the fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Product
HONDA — HONDA PASSPORT, PILOT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V896000·2024-11-27
Chrysler Recalls 2017-2018 Ram Trucks Due to Brake Control Unit Failure
Chrysler is recalling 2017-2018 Ram 2500, 3500, 4500, and 5500 trucks because the hydraulic control unit may fail, disabling anti-lock brakes and stability controls.
Product
RAM — RAM 5500, 2500, 4500, 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V899000·2024-11-27
Keystone Recalls 2025 Arcadia and Cougar Trailers for Hitch Fastener Issue
Keystone is recalling 2025 Arcadia and Cougar trailers because improperly tightened pin box fasteners may loosen, allowing the trailer to detach and increasing crash risk.
Product
KEYSTONE — KEYSTONE COUGAR, ARCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0373-2025·2024-11-27
Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare recalls peritoneal dialysis transfer sets (Part Number 5C4482) due to potential contamination with polychlorinated biphenyls (PCBs). The recall affects 2.7 million units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0379-2025·2024-11-27
Baxter MiniCap Dialysis Transfer Sets Recalled for PCB Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets used in peritoneal dialysis due to potential exposure to polychlorinated biphenyls (PCBs). About 62,394 units distributed worldwide may be affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2025·2024-11-27
Posi-Stop 25-Gauge Injection Needles Recalled for Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop 25-Gauge injection needles because some units contain manufacturing debris that blocks the needle's inner diameter, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2025·2024-11-27
CAIRE FreeStyle Comfort portable oxygen concentrator battery recharge failure
Caire Inc. is recalling 26 CAIRE FreeStyle Comfort portable oxygen concentrators due to potential battery recharge failure. Affected units identified by serial number may not charge properly.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24C002000·2024-11-27
Nuna Rava Child Seat Recall for Harness Adjuster Defect
Nuna is recalling Rava child seats where debris may cause the harness adjuster to fail, potentially leaving the harness loose in a crash.
Product
CHILD SEAT:HARNESS:FRONT ADJUSTER BUTTON/RELEASE MECHANISM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V898000·2024-11-27
Audi plug-in hybrid high voltage batteries can overheat
Volkswagen is recalling certain 2022-2023 Audi Q5 PHEV and 2022 Audi A7 PHEV vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2025·2024-11-27
Posi-Stop Injection Needles Recalled Due to Manufacturing Debris Blocking Injection Flow
Hobbs Medical recalls Posi-Stop injection needles because manufacturing debris can block the needle, preventing injection solutions from flowing properly. Affected units were distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0496-2025·2024-11-27
Siemens Atellica CH Cuvette Segment manufacturing defect may impact lab test accuracy
Manufacturing defects in Siemens Atellica CH Cuvette Segments may cause inaccurate laboratory test results for seven analytes across 9,729 units.
Product
Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain and incubate the sample reaction volumes and present them to each processing step. Siemens Material Number(SMN): 11099326 All lots starting with N15 or 15 are expected to have the defect.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls found in similar devices.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2025·2024-11-27
FDA Recalls Posi-Stop Injection Needles Due to Manufacturing Debris
Hobbs Medical is recalling Posi-Stop Injection Needles (25 gauge) because some units contain debris in the needle shaft that blocks injection solution flow.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0145-2025·2024-11-27
La Bonne Vie Camembert cheese recalled for potential Listeria contamination
La Bonne Vie Camembert 8oz cheese (UPC 820581678616, BBD 12/24/2024) is being recalled due to potential Listeria monocytogenes contamination. Approximately 70 cases were distributed across 12 U.S. states.
Product
La Bonne Vie Camembert 8oz UPC 820581678616; 6 retail units per case
Category
Food
Distribution
12 states
HighFDA (Food)·F-0141-2025·2024-11-27
Great Value Cinnamon Rolls Recalled for Plastic Contamination Nationwide
The JM Smucker Company is recalling Great Value Cinnamon Rolls nationwide due to possible plastic pieces in the product. Consumers should not consume affected units.
Product
Great Value Cinnamon Rolls 16.5oz UPC 078742201160, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0061-2025·2024-11-27
Lisinopril 10 mg Tablets Recalled for Metal Fragment Contamination
Evaric Pharmaceuticals is recalling Lisinopril 10 mg tablets after a metal fragment was found embedded in a tablet. The affected lot (241103) was distributed nationwide; contact your pharmacist if you have this medication.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2025·2024-11-27
JuggerLoc/ToggleLoc 2.9mm Drill Guide Warping in Packaging
Biomet's JuggerLoc/ToggleLoc 2.9mm Drill Guide may warp when removed from packaging, potentially extending surgical time or causing tissue damage requiring intervention.
Product
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24E100000·2024-11-27
Chrysler Recalls Brake Hydraulic Control Units Due to System Failure Risk
Chrysler is recalling specific MOPAR Brake Hydraulic Control Units that may fail, causing loss of anti-lock brakes, stability control, and traction control.
Product
SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2025·2024-11-27
Ramipril Capsule Medication Recalled Over Unapproved Vendor Manufacturing Deviations
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0468-2025·2024-11-27
Posi-Stop Injection Needles Recalled for Manufacturing Debris Blocking Flow
Hobbs Medical is recalling Posi-Stop Injection Needles because manufacturing debris blocks the needle, preventing injection solutions from flowing properly. The 70 affected units were distributed to healthcare facilities in multiple U.S. states and Canada.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2025·2024-11-27
CAIRE FreeStyle Comfort Portable Oxygen Concentrator Battery Recharge Failure
Six CAIRE FreeStyle Comfort oxygen concentrators may fail to recharge their batteries, potentially affecting portable use of these medical devices. Caire, Inc. is recalling affected units worldwide.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-103.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0049-2025·2024-11-27
Guaifenesin-Dextromethorphan Cough Syrup Recalled for Failed Impurity Specifications
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Product
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Category
Drug
Distribution
Distributed nationwide