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 Jan 20, 2016

Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood…

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

ArthroCare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…

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

Bayer Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…

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

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 20, 2016

TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED, 12-0.11OZ (3.2g)/ EA NET WT 1.34 oz (38g), UPC…

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

Twinings North America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 20, 2016

Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Smith & Nephew GENESIS(R) II/LEGION(TM) PATELLAR COMPONENT, RESURFACING ROUND, 32MM STANDARD, FOR CEMENTED USE ONLY…

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)

Food

Reported Jan 13, 2016

BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS: MILK, EGGS, WHEAT, SOY. MAY CONTAIN:…

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

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 6, 2016

Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Radiographic Transparency for Certain and External Connection Tapered Implants. Images that assist with measurements…

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

Biomet 3i, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 6, 2016

Friendly Farms Greek Peach Parfait Nonfat Yogurt net wt. 5.3 oz (150g) Distributed by ALDI Inc., Batavia, IL 60510

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

Ehrmann Arizona Dairy LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

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

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Vancomycin Screen Agar

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

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

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

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

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

IntellaTip MiFi XP Asymmetric (N4) Curve, 7/110/2.5/8-8 OUS; Material Number: M004EPM4500N40; Catalog number:…

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

Boston Scientific Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Cardinal Health Tiny Toes; 11470-010T Infant heel warmer

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

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

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2015

Fat Bastard Gourmet Chick Dip Honey Roasted Hickory Smoke Sassy Barbecue, Net Wt. 12 Fl. Oz. (375 ml), UPC 8 91929…

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

The Family Jewels LLC

FDA (openFDA food enforcement)

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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.