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 Sep 1, 2021

Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…

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

W. L. Gore & Associates Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,…

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

Ortho8, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

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

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 25, 2021

Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.

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

T & R Enterprises USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 25, 2021

The Aequalis Pyrocarbon Humeral Heads. Shoulder implant component. Sold OUS only: a) Catalog # DWH039 - Diameter 39 mm…

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

Tornier S.A.S.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513…

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

Bard Peripheral Vascular Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

ETEST IMIPENEM RELEBACTAM. in vitro diagnostic

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"

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

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 18, 2021

Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…

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

Iherb LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 18, 2021

Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 11, 2021

Regard NEWBORN KIT, LD00201j, Item Number: 830016010. Medical convenience kit which includes an infant heel warmer.

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

ROi CPS LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 11, 2021

Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent.

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

Stanbio Laboratory, LP

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 11, 2021

GlideScope Go Monitors

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Food

Reported Aug 4, 2021

Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC …

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

Del Monte Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic…

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

GE OEC Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 4, 2021

Backcountry Dried Apricots 9ounce plastic bag 12 packages per case

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

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

Heater Cooler Unit (HCU 30) The device supplies temperature-controlled water for cardioplegia heat exchangers and for…

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

Maquet Medical Systems USA

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 4, 2021

Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…

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

NOW Health Group Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 4, 2021

RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC…

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

Randall Foods, Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…

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

Sunrise Medical (US) LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC

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

Arthrex, Inc.

FDA (openFDA device enforcement)

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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.