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 Oct 15, 2014
Hostess Frosted Bagged Donettes, 11.25 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
Mars Chocolate North America Milk Chocolate M & M's Net Wt. 3.40 oz packed in a brown, 3 inch x 6.5 inch cardboard box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mars Chocolate North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Information Solutions LLC
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Richard-Allan Scientific Company
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2014
RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
LAP-BAND AP SYSTEM AP Large with Access Port, Allergan, LAP-BAND AP SYSTEM Access Port I. Product was distributed for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apollo Endosurgery Inc.
FDA (openFDA device enforcement)
Reported Oct 8, 2014
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Siemens Ysio Max system The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Condensed Skim Milk in bulk tanker (approximately 40,000 pounds per tanker load)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dairy Farmers
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 1, 2014
Lakewood Organic Fresh Pressed GMO Free Pure Apple Cold Pressed Not from Concentrate Juice Fruit 32 FL OZ (1 QT) 946 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Florida Bottling, Inc.
FDA (openFDA food enforcement)
Reported Oct 1, 2014
Circular Lock Screws, part # G826, lot # 11406. The Lock Screws are part of the Genesys Spine TiLock Pedicle Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genesys Orthopedics Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nanosphere, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pdg Product Design Group Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peters Surgical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
No packaging. The device is a computed tomography scanner. Intended to provide corss sectional images of the human body…
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)
Reported Oct 1, 2014
Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare 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.