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.
Reported Aug 1, 2012
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tripath Imaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Standard Process, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 25, 2012
Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Safedraw Venous Close Loop System, Blood Sampling Set, packaged in a tyvek bag, Model/Part Number 688695, Argon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Coca Cola Zero, 20 fl. oz., The Coca Cola Company.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coca-Cola Refreshments, USA Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Jimmy Peppers Hot Cherry Sliced Peppers, 1 gallon plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cosmo's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Edwards Lifesciences Rigid Suction Wand, sterile. Model numbers S033 and SPC2081. Product Usage: These suction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Focal SIM Planning of radiation therapy
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)
Reported Jul 18, 2012
Tom's Bacon Cheddar Fries, Flavored Corn and Potato Snacks, Net Wt., 2.75 oz (78.0g),
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snyder's - Lance Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.superDimension, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2012
TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 4, 2012
Hartmann Econolux Ref 416 105 Sterile Gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hartmann USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2012
Persimmon Hill Farm, Shiitake Mushroom Sauce, packaged in 8 oz/glass jars. The firm name on the label is Persimmon Hill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Persimmon Hill Farm Gourmet Foods
FDA (openFDA food enforcement)
Reported Jul 4, 2012
Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12 GAUGE BLUE NEEDLE RECTANGULAR FLANGE, 6" (15…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2012
Broaster Fish Coating, 96627, Ingredients: Corn Meal, Wheat Flour, Corn Crumbs, Salt, Spices, Paprika, Citric Acid,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Broaster Company, LLC
FDA (openFDA food enforcement)
Reported Jul 4, 2012
Reggano, Linguine and Parmesan Pasta Entree, NET WT 4.8 OZ(136g), UPC 4149813345, Distributed by ALDI Inc., Batavia, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TreeHouse Foods, Inc. / Bay Valley Foods
8 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2012
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2012
GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine. Used in Datex-Ohmeda Aestiva/5 Anesthesia Systems.
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 27, 2012
KERRY, 4 CHEESE SEAS 30506103, CONTAINS MILK, Net Wt 50 Lb (22.68 Kg), Item Number 30506103.465
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry Foods
61 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2012
SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR, 7.5" (19 CM) LONG. The Sarns High Flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2012
T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
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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.