State

Missouri product recalls

72,940 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,461
Critical: 1,333
Severe: 1,870
Most recent: 2026-09-09

Of the 8,461 recalls naming Missouri we have scored against our rubric, 1,333 (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 8,461 recalls whose distribution notice names Missouri specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4851–4875 of 81401

CriticalFDA (Food)·H-0089-2026·2025-10-29
Spinach free bowtie pasta kits recalled over potential Listeria contamination
Reser's Fine Foods is recalling 795 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.
Product
Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags of affected Bowtie Pasta and does not contain spinach. Kit is not sold directly to consumers.
Category
Food
Distribution
13 states
CriticalFDA (Food)·H-0149-2026·2025-10-29
Breakfast burritos recalled after cooked egg ingredient tested positive for Listeria
M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.
Product
Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0090-2026·2025-10-29
Bowtie pasta kits recalled over potential Listeria monocytogenes contamination
Reser's Fine Foods is recalling 3,252 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.
Product
Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bowtie Pasta, and it is not sold directly to consumers.
Category
Food
Distribution
13 states
CriticalFDA (Food)·H-0132-2026·2025-10-29
Shrimp scampi meals recalled over linguine linked to Listeria outbreak
Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.
Product
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0150-2026·2025-10-29
Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria
M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.
Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0154-2026·2025-10-29
IV burette sets recalled over missing internal shutoff valve component
ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.
Product
IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0070-2026·2025-10-29
Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors
B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.
Product
Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0088-2026·2025-10-29
Deli pasta salad recalled because it may contain Listeria monocytogenes
Sprouts Farmers Market is recalling Smoked Mozzarella Pasta Salad sold at deli counters and in grab-and-go containers because the product may contain Listeria monocytogenes.
Product
Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers at Deli counter and into 16oz plastic grab & go containers, weight dependent on customer request, UPC 2-15587-00000 (from service case) and 2-15786-00000 (from
Category
Food
Distribution
24 states
SevereNHTSA·25V737000·2025-10-29
Mazda CX-50 front suspension bolts may allow wheel detachment
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Product
MAZDA — MAZDA CX-50, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2026·2025-10-29
Gastric sump anti-reflux valves recalled after breakage complaints from excessive force
Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0112-2026·2025-10-29
Frozen cooked shrimp recalled across four brands over cesium 137 contamination
Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.
Product
Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
Category
Food
Distribution
34 states
HighFDA (Food)·H-0116-2026·2025-10-29
Frozen shrimp skewers recalled in expanded cesium 137 contamination action
Southwind Foods is recalling Great American branded frozen raw shrimp skewers made under insanitary conditions in which the product may have been contaminated with Cesium-137.
Product
Great American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
Category
Food
Distribution
34 states
HighFDA (Drugs)·D-0035-2026·2025-10-29
Alcohol prep pads recalled from one lot as a subpotent drug
Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.
Product
Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0232-2026·2025-10-29
Insulin pumps recalled over software defect causing unexpected correction bolus
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Product
t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0239-2026·2025-10-29
Automated microbiology systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0215-2026·2025-10-29
Clinical analyzer modules recalled over dilution factor software anomaly affecting results
Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0114-2026·2025-10-29
Frozen cooked salad shrimp recalled over possible cesium 137 contamination
Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.
Product
Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-0227-2026·2025-10-29
Bipolar hip heads recalled downstream after femoral components failed transit testing
Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.
Product
iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0210-2026·2025-10-29
Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0236-2026·2025-10-29
BACTEC FX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2026·2025-10-29
PVC stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0211-2026·2025-10-29
Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2026·2025-10-29
Immunoassay analyzers recalled over dilution factor anomaly affecting patient results
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxI 9000 Access Immunoassay Analyzer, Part Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0233-2026·2025-10-29
Oral thermometer probes recalled after being programmed with rectal configuration
Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.
Product
Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0235-2026·2025-10-29
Microbiology data systems recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
Category
Medical Device
Distribution
Distributed nationwide