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 Mar 30, 2016

Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2016

Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 30, 2016

NP Nutra Spinach Powder Organic SKU: 790 Net Weight: 22.72kg Gross Weight: 24kg Product of USA

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

NP Nutra

FDA (openFDA food enforcement)

Medical devices

Reported Mar 30, 2016

Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and…

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

Zimmer Spine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic…

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

Deerfield Imaging

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…

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 Mar 16, 2016

Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2016

Bertolli Extra Virgin Olive Oil, 8.5 oz. and Carapelli Extra Virgin Olive Oil, 25.5 oz., packaged in glass bottles.

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

DEOLEO USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2016

Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most…

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

Gi Supply

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2016

Living Tree Community Foods Organic Macadamia Nuts, 4 oz. plastic pouch. Certified Organic

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

Living Tree Community Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2016

Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10 is intended…

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 Mar 16, 2016

Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist…

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

Sedecal S.A.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quality control material…

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

TEM Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

M/L Taper Hip Prosthesis (Item: 00-7711-012-20, Lot: 62937093

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2016

Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…

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

Braga Organic Farms, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2016

Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle…

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

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, Used to support the upper and lower…

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

Maquet Cardiovascular US Sales, LLC

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.