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.
Reported Nov 8, 2023
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 8, 2023
Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Whole cantaloupe, Brand name Kandy 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eagle Produce LLC, dba Martori Farms
FDA (openFDA food enforcement)
Reported Nov 1, 2023
SOZO Bilateral Arm L-Dex Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impedimed Limited
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor
High riskUsing this product could cause serious injury, illness or death — stop using it now.Orgain
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Astral 100 and Astral 150 ventilators
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Oct 25, 2023
Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
Reported Oct 18, 2023
Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 18, 2023
Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g), plastic package (i.e.) Clamp shell, 8 package per case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairfield Gourmet Food Corp. d/b/a David's Cookies
FDA (openFDA food enforcement)
Reported Oct 18, 2023
LuLu Chinese Express Korean Noodles (Japchae) w/ Vegetables. Net Wt 16oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.JX Restaurants, Inc.
FDA (openFDA food enforcement)
Reported Oct 18, 2023
LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Little Oak Company Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 11, 2023
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
GS0008 2Y - Burn Pack - STL, Item Number 880082025
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ROi CPS LLC
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Oct 4, 2023
Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Perifix¿ / Epidural anesthesia set, medicated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
DJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Great Lakes Cheese, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 27, 2023
FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* Lining, Orange, size small, Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
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.