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.
Reported Mar 7, 2018
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2018
La Kansas City Baking Company Retira Productos De Carne Listos Para Consumir Producidos Sin El Beneficio De Inspeccin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Feb 28, 2018
Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Holsum Baking Company Warehouse
FDA (openFDA food enforcement)
Reported Feb 28, 2018
Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lemon Ginger Syrup, packaged in 100 mL or 250 mL glass bottle. 100 mL bottle has UPC 8 53142 00504 0. 250 mL bottle has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Improper Goods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2018
EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Little Rapids Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Artis oneFloor-mounted system for uncompromised imaging; Artis one, Interventional fluoroscopic x-ray system, Artis one…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Feb 14, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Peripheral Diamondback 1.25 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chobani
FDA (openFDA food enforcement)
Reported Feb 14, 2018
SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J F C International Inc.
FDA (openFDA food enforcement)
Reported Feb 14, 2018
TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Feb 14, 2018
SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventura Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2018
DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dollar General Corporation, Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, 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.