All recall categories

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.

Medical devices

Reported Jul 28, 2021

Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Respironics California, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 - Product Usage: intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 21, 2021

Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs per case; 2 cups…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bazzini LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 21, 2021

Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Canon Medical System, USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis Corporation

FDA (openFDA device enforcement)

Drugs

Reported Jul 21, 2021

B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutritional, Inc., Melbourne, FL 32935, NDC…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Grato Holdings, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jul 21, 2021

EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit cup cementless 46mm dia incl. central hole…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Implantcast GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mercedes Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Owen Mumford USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RanD S.r.l.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 14, 2021

Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beechnut Nutrition

FDA (openFDA food enforcement)

Medical devices

Reported Jul 14, 2021

FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…

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)

Medical devices

Reported Jul 14, 2021

Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Heart Valves Division

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

The ADVIA Chemistry XPT Chemistry System, Siemens Material Number (SMN) 10723034, is an automated, clinical chemistry…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Jul 14, 2021

Yakult Nonfat Probiotic Drink; Live and active Lactobacillus casei Shitota; 2.7 FL. OZ. (80 mL), 5 individual bottles…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Yakult U.S.A. Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 7, 2021

Guan's Seafood Mushroom - hetre blanc UPC 8 5926700750 1 150 g clear plastic package with green bottom; Product code…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

California Terra Garden, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 7, 2021

Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Exactech, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 7, 2021

Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

H & H Products Company

FDA (openFDA food enforcement)

Food

Reported Jul 7, 2021

Smilin' Bob's Key West Style Smoked Fish Dip Original 8 oz and 15.5 oz plastic container 12 per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lakeview Farms LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 7, 2021

Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Quidel Corporation

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.