State

Missouri product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2876–2900 of 81397

SevereFDA (Devices)·Z-1546-2026·2026-03-18
TRUE METRIX PRO manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX PRO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE MET
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1547-2026·2026-03-18
TRUE METRIX AIR manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX AIR blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1545-2026·2026-03-18
TRUE METRIX manuals recalled as Class I over E-5 error code guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01, Leader TRUE METRIX Meter Only/RE4002-40, CVS TRUE METRIX Kit/RE4007-01SB, GN
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1548-2026·2026-03-18
TRUE METRIX GO manuals recalled as Class I over E-5 error guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX GO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007-01, Meijer TRUE METRIX GO Kit/RF4019-01, Fred's Phamarcy TRUE METRIX GO Kit/R
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0546-2026·2026-03-18
Rosabella Brand Moringa Dietary Supplement Capsules Contaminated with Salmonella
Ambrosia Brands LLC is recalling Rosabella brand Moringa dietary supplement capsules nationwide and internationally because the product may be contaminated with Salmonella.
Product
Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min befo
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2026·2026-03-18
Link Endo-Model plateau 15-8521/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2026·2026-03-18
Vital Sync remote monitoring may not receive bedside monitor alarms
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Product
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 /
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1564-2026·2026-03-18
Medline surgical drapes may delaminate prematurely after recommended laundering
Medline is recalling five surgical drape products because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1555-2026·2026-03-18
Artelon FlexBand Plus implants failed bacterial endotoxin testing
International Life Sciences is recalling Artelon FlexBand Plus, refs 41054 and 41057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Plus Ref: 41054 & 41057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1558-2026·2026-03-18
Lutronic Clarity II laser system reported sparking and popping during use
Lutronic is recalling the CLARITY II Laser System after reports of devices sparking or popping and potentially burning patients.
Product
CLARITY II Laser System; Model No. 1110200210.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1526-2026·2026-03-18
GEM Premier 5000 PAK part 00055360010 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2026·2026-03-18
Link Endo-Model SL component 16-2840/02 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/02 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2026·2026-03-18
Link Endo-Model plateau 15-8521/09 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/09 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/09;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1539-2026·2026-03-18
GEM Premier 5000 cartridges may eject repeatedly during analyzer warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 analyzers after confirmed complaints that GEM PAK cartridges may show increased Process Control Solution Not Detected errors during warm-up.
Product
GEM Premier 5000; Model No. 00055430010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2026·2026-03-18
Link Endo-Model SL component 16-2840/05 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/05 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1551-2026·2026-03-18
EndoVive PEG kits recalled over compromised ChloraPrep swabstick seals
Boston Scientific is recalling EndoVive Safety PEG Kits containing BD ChloraPrep Triple Swabsticks because open or compromised seals on the swabstick packaging could cause loss of sterility.
Product
EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2026·2026-03-18
Raz shower commode chair seat may be reinstalled without engaging brackets
Raz Design is recalling several Mobile Shower Commode Chair models because a vendor modification means the seat may be reinstalled without properly engaging the outside rear seat brackets that hold it in place.
Product
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2026·2026-03-18
Artelon FlexBand Twist anchors failed bacterial endotoxin testing
International Life Sciences is recalling the Artelon FlexBand Twist .12, ref TW012, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1524-2026·2026-03-18
GEM Premier 5000 PAK part 00055360004 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK, Part No. 00055360004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2026·2026-03-18
Beckman Coulter AU5800 analyzer may stop analyzing after database errors
Beckman Coulter is recalling Chemistry Analyzer AU5800 units because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1527-2026·2026-03-18
GEM Premier 5000 PAK part 00055360011 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2026·2026-03-18
IBA proton therapy system may not interrupt beam when gating fails
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Product
IBA Proton Therapy System - PROTEUS 235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0548-2026·2026-03-18
Vegetarian Chicken Flavor Ramen Express contains undeclared Yellow #5
Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.
Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Palm oil***" Contains: Wheat, Soy. UPC 8 10037 81004 2 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
Category
Food
Distribution
32 states
HighFDA (Devices)·Z-1552-2026·2026-03-18
Beckman Coulter DxC 700 AU analyzer may stop analyzing after errors
Beckman Coulter is recalling DxC 700 AU analyzers because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
DxC 700 AU, REF: B86444, B86446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1525-2026·2026-03-18
GEM Premier 5000 PAK part 00055360008 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360008.
Category
Medical Device
Distribution
Distributed nationwide