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 Dec 14, 2022
Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intersect ENT, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
FDA (openFDA food enforcement)
Reported Dec 14, 2022
IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Accelerate PhenoTest BC kit REF 10101018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accelerate Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Alcon Custom Pak Surgical Procedure Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Dec 7, 2022
CMV IgM EIA, in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2022
INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
eSuction Small Cavity, Model ET2005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Endo-Therapeutics, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Hamilton-C6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Nov 30, 2022
K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Nov 30, 2022
regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ROi CPS LLC
39 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2022
The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tomato Head Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altimate Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Hill-Rom Progressa Bed System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
125 series iGO2 Portable Oxygen Concentrator-indicated for the administration of supplemental oxygen. Models: 125D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeVilbiss Healthcare LLC
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Disposable Surgical Level 3 Gown, Size/Product Code: Large/GWS-03-L-B, XLarge/GWS-03-XL-B, XXLarge/GWS-03-XXL-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Texas Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
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Other states
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.