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 Jul 20, 2022
Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Isopure Corp.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.) 1.13kg. Item Number 803320R. UPC 51497 14360. Light panko…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market Day Local Inc.
FDA (openFDA food enforcement)
Reported Jul 20, 2022
MiniMed 620G Insulin Pump (O.U.S. version)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Omnera 400T Digital Radiographic System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arcoma AB
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
ABL800 Flex Analyzer Model Numbers 393-800 and 393-801
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jul 13, 2022
RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rayner Intraocular Lenses Ltd.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Independent Beverage Company LLC
FDA (openFDA food enforcement)
Reported Jul 6, 2022
Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Volcano Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2022
Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 29, 2022
Alcon Clareon IOL with AutonoMe Delivery System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Laboratories Ireland, Ltd.
FDA (openFDA device enforcement)
Reported Jun 29, 2022
REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Flow-c Anesthesia System : intended for use in administering anesthesia while controlling the entire ventilation of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Getinge USA Sales Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms Retail Inc.
FDA (openFDA food enforcement)
Reported Jun 22, 2022
illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 22, 2022
Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2022
(1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BSN Medical Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2022
Back up batteries in Ventilators labeled as the following: a. CARESCAPE R860 Ventilators (K142679) b. ENGSTROM…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2022
dibz Lunch Blox. Entree, Grain, Veggie, Fruit
High riskUsing this product could cause serious injury, illness or death — stop using it now.General Mills James Ford Bell Technical Center
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.