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 Dec 25, 2019
QuickTox 5 Panel Drug Screen DipCard
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ameditech Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
CrossCath Support Catheter, RPN CXC3.0-1.9-14-90-P-NS-0, Order Number G51572 For diagnostic and interventional vascular…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
41 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
MRIdian Linac Radiation Therapy System Model 10000 and 20000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Fortune Fish & Gourmet fresh Atlantic salmon, whole, filleted, and filleted without belly sold by weight in cardboard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fortune International, LLC dba Fortune Fish & Gourmet LLC
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frog Hollow Farm
FDA (openFDA food enforcement)
Reported Dec 11, 2019
EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NDDd Medical Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Great Value Old Fashioned Glazed Donuts packaged in a paperboard box with cellophane window and each box contains 6…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.United States Bakery Corp.
FDA (openFDA food enforcement)
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
SOMATOM go.Top, Models 11061640 & 11061648- a Computer tomography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2019
Missa Bay, LLC Recalls Salad Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay LLC
USDA FSIS
Reported Nov 20, 2019
Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Science, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
GSMS: Ranitidine Capsules 150 mg, Rx only, 500 count bottles (NDC 51407-097-05) Manufactured by Novitium Pharma LLC, 70…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ORTHOFIX Catalogue Number: ref 11007, drill bit diameter 4.8 MM LENGTH 280 MM, RX ONLY, Non Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix Srl
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
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.