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 12, 2014

3.5mm Locking Cortical Bone Screw, T15 Hexalobe, Self Tapping, 20mm Part No. 00-0903-2620 OrthoPediatrics Pediloc"…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470,…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2014

Walmart Great Value Tex Mex Trail Mix, Net Wt 28 oz (793g), Distributed by Wal Mart Stores, Inc., Bentonville, AR,…

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

Ann's House

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2014

Simplexa Flu A/B & RSV Direct assay, Model MOL2650. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is…

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

Focus Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140,…

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

Navilyst Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Brilliance iCT, Brilliance 64 and Brilliance Big Bore The Brilliance iCT, Brilliance 64 and Brilliance Big Bore are…

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

Philips Medical Systems (Cleveland) Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or…

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

Spacelabs Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Teflon Tube, sterile T2 Humerus System Stryker Trauma GmbH Prof Kuntscher Str 1-5 24232 Sconkidrchen, Germany…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jan 30, 2014

Missouri Firm Recalls Chicken Salad Products Due To Misbranding and Undeclared Allergen

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

Walker's Food Products Co.

USDA FSIS

Medical devices

Reported Jan 29, 2014

AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.

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

Churchill Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a…

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

Davol, Inc., Subs. C. R. Bard, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

VITROS Chemistry Products COCM Reagent

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 22, 2014

Metformin Hydrochloride USP, Active Pharmaceutical Ingredient for manufacturing, processing or re-packing use only, 25…

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

Betachem, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 22, 2014

Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…

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

Ge Healthcare It

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2014

Hot Smoked Wine Maple Salmon, Item HS-B, vacuum packaged and either frozen or refrigerated, ranging in size between…

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

Josephson's Smokehouse

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2014

Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…

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

Leica Biosystems Newcastle Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

pO2 D999 membrane units. Distributed by Radiometer America, Inc., Westlake, OH 44145 pO2 membrane units, ordering…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only

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

ArthroCare Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

REF 42-411571 QTY 1 CATALOG CAUTION. SEE INSTRUCTIONS FOR USE SIGNATURE M PKA GDE/MDL SET SML-MP DD.....R-FEB55RKA-T…

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

Materialise USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Catalys Precision Laser System (United States) - Catalys-U: Catalys Precision Laser System (International) - Catalys I…

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

Optimedica Corporation

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.