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 Apr 24, 2019

Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: The Alinity i processing module is a fully automated…

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

Abbott GmbH & Co. KG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are…

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

Bioventus, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T

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

Integra LifeSciences Corp.

25 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2019

NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton

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

Little Red Rooster Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2019

14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Obturator (long cone), Part number 25162 Product Usage: The obturator is a component of the Flex Rectoscope which is an…

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

Medrobotics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

SORIN Heater-Cooler System 3T, REF 16-02-85 Intended for use with a Stockert/Sorin S3/S5/C5 heart-lung machine and/or…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…

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)

Medical devices

Reported Apr 17, 2019

ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal…

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

ulrich medical USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2019

Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Beaver Visitec

FDA (openFDA device enforcement)

Food

Reported Apr 10, 2019

Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame…

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

Century Snacks LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 10, 2019

McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Cypress Medical Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Accelerate Pheno system, with Accelerate Pheno System Software 1.2.1 - 1.3.1, PSW000012B Product Usage: The Accelerate…

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

Accelerate Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or…

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

Beaver Visitec

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the…

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

Fenwal Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 3, 2019

Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7…

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

ProThera, Inc. dba SFI USA

FDA (openFDA food enforcement)

Food

Reported Mar 27, 2019

Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton, 12 retail units per wholesale case. UPC# 70038…

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 27, 2019

smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1 SIZE, STEM, REF 713552510

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

Smith & Nephew, Inc.

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.