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 Feb 20, 2013

GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The T-piece Resuscitation System [ventilator, emergency…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2013

Stringless Sugar Snap Peas, Sunny Shores' Mann's. Net Wt 8 oz (227 g); Perishable, Preservative Free, keep…

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

Mann Packing Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2013

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2013

St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…

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

St Jude Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…

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

Diagnostic Hybrids Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage: Universal Fluoroscopic Applications

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

Philips Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Oxoid Antimicrobial Susceptibility Test Discs, Aztreonam 30 ug, IVD, REF CT0264B, Oxoid Ltd., UK, oxoid@thrmofisher.com…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…

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

Synthes USA HQ, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…

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

Cordis Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774…

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

EonNutra, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

AdvantageSim MD versions 7.4 through 7.6, Model 5160092-2 Version 7.4, 5160092-3 Version 7.5, 5160092-4 version 7.6.

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt.…

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

Jiffy Food Service, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general…

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

Philips Healthcare Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Kinnikinnick Pie Crust (frozen), Weight: 290 g/10 oz, Qty/Pkg: 2, Product packaged in a cardboard box with printed…

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

United Natural Foods, Inc. - Greenwood

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2013

DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.

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

DePuy Spine, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 30, 2013

Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***BLACK BEAR***of the BLACK FOREST*** Naturally…

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

Marine Harvest USA, LLC

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2013

Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2013

Sarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.5 in (24 cm) long The…

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

Terumo Cardiovascular Systems Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 23, 2013

Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.

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

Woodstock Farms

FDA (openFDA food enforcement)

Food

Reported Jan 16, 2013

Cherry tomatoes packaged in 1 pint clear, plastic clamshells. The clamshells are packaged either 9/1-pint clamshells or…

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

Capital City Fruit Co.

FDA (openFDA food enforcement)

Food

Reported Jan 16, 2013

Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS…

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

Multiexport Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 9, 2013

Fresh Express brand, Fresh Spinach, 9 oz.

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

Fresh Express Incorporated

FDA (openFDA food 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.