Recalls distributed in Florida
These notices name Florida 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.
6,421 stored notices name Florida, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Jan 31, 2024
PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
R&B Chocolate Chips Croissant Twist
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lecoq Cuisine Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 31, 2024
Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Publix Custom Made Sub Sandwiches, variable weights and sizes, individually wrapped in paper, intended for immediate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Publix Super Markets, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 31, 2024
Sedecal X Optima URS digital mobile diagnostic x-ray system. A a stationary x-ray unit with a universal swivel arm. It…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal Sa
FDA (openFDA device enforcement)
Reported Jan 31, 2024
TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Atrial Fibrillation Division, Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Tapee Tea packaged in paper packets - 5 packets per bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Wiedemann Company LLC
FDA (openFDA food enforcement)
Reported Jan 24, 2024
FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Lettuce in clear plastic 2lb bags.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 24, 2024
VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Ministry of Snacks Sweet and Savory Collection #8700
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phase Scientific International Limited
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Neiman Marcus Christmas Petit Fours 24pc
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sweet Shop Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Wellsley Farms Assorted Mini Quiches NET WT 36 OZ (2LB 4 OZ) 1.02kb Keep Frozen UPC: 8867002630. Packaged in plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Fillo Factory Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TreeHouse Foods, Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 24, 2024
DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, store in ambient temperatures
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventura Foods LLC
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CD11b APC: ASR, REF: 340936, and CE, REF: 333143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jan 17, 2024
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
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.