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 48,122 notices were distributed nationwide, so they reach Missouri too — those are in the archive.

Medical devices

Reported Jun 14, 2017

Oxygen Masks, Elongated (under chin), Adult Med Conc., No Tubing, Product Code 104-E;

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

ConvaTec, Inc.

17 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 14, 2017

Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt. 14 ounce. Retail package UPC 0 43301 61119 3.

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

Lamb Weston Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 14, 2017

Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Food

Reported Jun 14, 2017

STILL RIDING FOODS GLUTEN FREE PIZZA CRUST; Sold in the following package sizes: 36/9" NET WT 15lbs (6.80kg); 12/12"…

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

Still Riding Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 14, 2017

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

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

Teleflex Medical

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 13, 2017

Joseph Seviroli Inc. Recalls Beef Products Due to Misbranding and Undeclared Allergens

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

Seviroli Foods, LLC

USDA FSIS

Medical devices

Reported Jun 7, 2017

The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

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

Cardinal Scale Mfg Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

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

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 7, 2017

Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail…

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

Trident Seafoods Corp. - Island Enterprise M/V

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 31, 2017

Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Food

Reported May 31, 2017

Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…

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

Phoenix Food, LLC

FDA (openFDA food enforcement)

Food

Reported May 31, 2017

Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement,…

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

RB Manufacturing LLC

FDA (openFDA food enforcement)

Food

Reported May 31, 2017

ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…

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

Rich Products Corp.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 31, 2017

Herbal Tea Variety 120 ml/pouch, 40 pouches/case

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

U S Deer Antlers Export & Import

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2017

SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600

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

Biomet Microfixation, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

GIZA Vertebral Body Replacement

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

Eden Spine Europe SA

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…

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

Almore International Inc.

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.