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 Dec 5, 2012
Kroger Deluxe French Vanilla Magnifique Ice Cream, 48 FL OZ laminated carton. INGREDIENTS: MILK, CREAM,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 5, 2012
NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovative Magnetic Resonance Imaging Systems Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD¿ Patient Size:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Screw Tulip , 6.25mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
SenTec V-Sign Membrane Changer (VS-MC), 9 pieces. The SenTec V-Sign Membrane Changer is indicated for use with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sentec AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Inspan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SpineFrontier, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Salted in-shell Peanuts under the following. Salted in Shell PeanutsGless Ranch Label, Item Number 450-175, Pack Size…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Torn & Glasser Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2012
Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Signs Colorado Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Signs Devices, a GE Healthcare Company
FDA (openFDA device enforcement)
Reported Nov 21, 2012
PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management System is a selfcontained, dual channel system for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 071039) Cliniqa Liquid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Belfonte Home Run Sundae Ice Cream, A Baseball Nut Blend of Chocolate Peanuts, Chocolate Coated Pretzels, and a Thick…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Belfonte Ice Cream & Dairy Foods Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Dole American Blend; Iceberg, Romaine, Red Cabbage, Carrots and Radishes. Net Wt. 12 oz. (340g) UPC 0 71430 00933 8…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2012
ILLlCO¿ MIS Posterior Fixation System, Bone-screw Internal Spinal Fixation System, Orthosis, Spinal Pedical Fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2012
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartsine Technologies, Limited
FDA (openFDA device enforcement)
Reported Nov 7, 2012
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Missouri recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.