All recall categories

Recalls distributed in Missouri

These notices name Missouri in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,082 stored notices name Missouri, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Missouri too — those are in the archive.

Medical devices

Reported Aug 14, 2024

American Contract Systems Hand Pack convenience kit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Contract Systems, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2024

Premo King Club Footlong 11.5oz, clear plastic, UPC 612510094259, 4 retail packages per wholesale case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lipari Foods Operating Company, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 14, 2024

Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2024

Wiers Farm - Whole Salad Cucumbers bagged in 2lb plastic bags, 10 bags per carton

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wiers Farm Inc.

26 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hoff & Pepper, Co. LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2024

Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medivance Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Prophet Premium Blends, LLC

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2024

Abbott Infinity 5, Implantable Pulse Generator, REF: 6660, SterileEO, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX analyzers are intended for: " In Vitro testing of samples…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2024

Aahu Barah Apricot Roll; 14 oz; sold in clear plastic bags (6 inch x 8 inch) packing with the Aaha Barah label on the…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Global Commodities Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2024

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C. Krueger Finest Baked Goods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Echonous Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2024

Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MICROspecialties, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.