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 Aug 7, 2013

LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-shaft portion of the…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

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

HeartWare Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2013

OSKRI, Coconut Bar Dark Chocolate, Net Wt. 1.9 oz ( 53g), UPC 6 66016 30070 3. Ingredients: Coconuts 55%, Rice Syrup,…

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

Oskri Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2013

Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient…

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

Picis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…

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

Tosoh Smd Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Sodium Bicarbonate, USP Provided bulk as raw material - label not applicable according to firm Dialysis Grade 1.5…

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

Church & Dwight Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved…

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

Ethicon Endo-Surgery Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluation of the extrinsic…

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

Instrumentation Laboratory Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides…

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

National Biological Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Rultract Retractor Ratchet Cover Plate Distributed by Pemco, Inc., Cleveland, OH 44131 Surgical retractor used to lift…

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

Pemco Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2013

B-CrossLaps/serum (B-CTx in serum) REF 11972308 160 100 tests Immunoassay for the in vitro quantitative determination…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2013

Somersault Pacific Sea Salt flavor, crunchy nuggets baked with sunflower seeds and toasted grains. 1 oz. packages sold…

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

Somersault Snack Co., LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2013

nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has…

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

Staar Surgical Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…

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

Terumo Cardiovascular Systems Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2013

Mango (Fresh Cut): Del Monte brand slices, 32 oz., UPC 7-62357-07532-1, 32 oz., UPC 7-17524 72503-5; 16 oz., UPC…

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

Del Monte Fresh Produce North America, Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2013

Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2013

***REF C7120***APEX Arthroscopy Tubing Set. Intended for use for joint irrigation and dissention during arthroscopic…

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

Linvatec Corp. dba ConMed Linvatec

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2013

Eagle Premium, Snack Shoppe, Pistachios, in-shell pistachios, packaged in 2-oz (UPC 4262500705) and 5.25-oz (UPC…

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

Palmer Candy Co.

FDA (openFDA food enforcement)

Food

Reported Jul 17, 2013

R.L. Schreiber Batter Mix, 2.5 lb packaged in white flexible plastic bag, 12 bags per case.

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

R.l. Schreiber Inc. - Lebanon

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2013

Bigliani/Flatow¿ The Complete Shoulder Solution, Humeral Stem Provisional 12mm x 170mm This reusable trial device is…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2013

Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…

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

Cheryls

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2013

HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.

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

Clorox Healthcare Holdings, LLC (dba HealthLink)

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2013

1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product…

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

Ortho-Clinical Diagnostics

4 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.