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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 48,100 notices were distributed nationwide, so they reach Missouri too — those are in the archive.

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

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

ICU Medical, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

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

Nova Ortho-Med Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Microsurgical Operating Room Tables;7300B (18-350-70);

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

Mizuho America, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 23, 2020

Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205

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

SCA Pharmaceuticals

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 16, 2020

Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture of Membrane Test ROM-5025, ROM-6025

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

Clinical Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

MAC VU360, Electrocardiograph

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

Hy-Vee, Short Cuts, Grill Ready Veggie Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc,…

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

Hy-Vee Stores Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during…

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

Mani, Inc. - Kiyohara Facility

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g

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

The Kroger Co.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

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

Welch Allyn, Inc/mortara

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or…

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

CME America, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2020

Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 9, 2020

Regard - Product Usage: Obstetric Gynecologic specialized manual instrument. Labor and delivery kits.

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

ROi CPS LLC

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2020

Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura &…

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

Tanimura & Antle

FDA (openFDA food enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

MEVION S250i, MEVION S250; Proton Radiation Treatment System - Product Usage: intended to deliver proton radiation…

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

Mevion Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60…

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

Viewray, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 2, 2020

Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3

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

Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers

FDA (openFDA food 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.