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 27, 2014
Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2014
TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Allegro Original Marinade, 12.7 fl oz (375 mL), UPC 0 74964 00100 7
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allegro Fine Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 20, 2014
VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosound Esaote, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Codman & Shurtleff, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Ronzoni Roasted Garlic Fettuccine Net Wt. 12 OZ. Enriched Macaroni Product shelf-stable packed in blue paperboard box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EBRO North America dba New World Pasta
FDA (openFDA food enforcement)
Reported Aug 20, 2014
Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Positioning Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 20, 2014
IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advandx Inc.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe, BZK Swabs, Sterile, Rx only, Teleflex Medical Product…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Serrated Soft Tissue Shields. Orthopedic surgical instruments, part of the Silex Sacroiliac Fusion System. The soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Aug 6, 2014
DeRoyal KNEE ARTHROSCOPY PACK, REF 89-6192.04, 1 Per Pack, Distributed by: DeRoyal Industries, Inc.; Manufacturer:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Aug 6, 2014
MC-500 Multicolor Laser Photocoagulator; Distributed by NIDEK Inc. Manufactured by NIDEK CO., Ltd, Japan. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Professional Bak-klene All Purpose No-Stick Bakery Spray, packaged in 14-oz. aerosol cans.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Plaze Inc.
FDA (openFDA food enforcement)
Reported Aug 6, 2014
Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw System Sets, Implants, and Instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Small Bone Innovations
FDA (openFDA device enforcement)
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Aug 6, 2014
IPM Wound Gel Rx Wound Dressing IPM Wound Gel is indicated for the management of wound healing.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellspring Pharmaceutical Corporation
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.