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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 Mar 5, 2014

GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…

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

Ortho-Clinical Diagnostics

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…

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

Philips Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System

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

Smith & Nephew Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…

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

Winco Mfg., LLC

3 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 26, 2014

California Firm Recalls Canadian Liver P,tE Products Produced Without Import Inspection

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

California Firm

USDA FSIS

Medical devices

Reported Feb 26, 2014

Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

GE Healthcare, PET Discovery 610, Discovery 710, Discovery 600 and Discovery 690. The GE Discovery XR and XA Systems…

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 Feb 26, 2014

Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2014

Digestive enzyme capsules sold under the NOW Foods, Beeyoutiful, Best in Nature, Bluegrass Naturals Vitamin Company,…

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

NOW Foods

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2014

Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device with wheels that is intended for medical purposes…

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

The Standing Company

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2014

Boston Scientific, 2.5mm Coyote" OVER-THE-WIRE PTA Balloon Dilation Catheter, UPN# H74939186251210, Catalog #…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2014

Panko Style Bread Crumbs net wt. 350g 12.5 oz. gluten free, dairy free, nut free

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

Braum's Ice Cream and Dairy

FDA (openFDA food enforcement)

Food

Reported Feb 19, 2014

Farm To Market Bread Co. San Francisco Sourdough, net weight 1 lb., unbleached enriched flour, water, sea salt, vitamin…

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

Farm To Market Bread Co. Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 19, 2014

Pringles, the Original, Net Weight 5.68 oz (161 g) UPC code 0 38000 84496 6 Ingredients: INGREDIENTS: DRIED POTATOES,…

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

Kellogg Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2014

Medtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100, Rx only, STERILE A, QTY: 1 EA, Medtronic Sofamor Danek, USA,…

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

Medtronic Sofamor Danek USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2014

GEMINI TF Big Bore PET/CT, Computer Tomography System, Philips Healthcare System, Cleveland, OH

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2014

The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The…

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

Sysmex America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

B. Braun AccuFlo Elastomeric Infusion Pump 200ML/H 100 ML Generally used for delivery of antibiotic and local…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 12, 2014

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's…

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

Dr. Reddy's Laboratories, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 12, 2014

XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as…

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

Medtronic Advanced Energy, LLC

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.