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 Dec 9, 2020

Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional…

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

Talladium Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2020

Minute Maid STRAWBERRY LEMONADE FLAVORED WITH OTHER NATURAL FLAVORS 59 FL OZ (1.8 QT) 1.75 L PRODUCED FOR THE COCA-COLA…

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

The Coca-Cola Company

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da…

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

Advanced Bionics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 2, 2020

HQO High Quality Organics Organic Thyme Leaves, Whole Net Weight 30 lbs., 500 lbs. High Quality Organics 1201 Moya…

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

High Quality Organics

FDA (openFDA food enforcement)

Medical devices

Reported Dec 2, 2020

Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…

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

Hill-Rom Manufacturing, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

MEVION S250i, MEVION S250; Proton Radiation Treatment System - Product Usage: intended to deliver proton radiation…

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

Mevion Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60…

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

Viewray, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…

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

Art Of Tea

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Alpen Clinic 100 Carbide Instruments (R100057C)

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

Coltene Whaledent Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Denali Ingredients Cream Tech 250 Sour Cream Stabilizer, Item 500120-1014, 50 lb. bag. Storage: For maximum Freshness…

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

Denali Ingredients LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

VNS Therapy¿ AspireSR¿ Generator

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Nov 25, 2020

Metformin HCl Extended Release Tablets USP 500 mg, Generic for : Glucophage XR, Pkg Size 100, Mfg: Time-Cap Labs, Inc.;…

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

Preferred Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 25, 2020

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

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

Thomas Scientific

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…

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

Aesthetics Biomedical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 18, 2020

TROPIQUE ASSORTED FRUIT JELLY BAG 30/9PCS/10.06oz and TROPIQUE JELLY ANIMAL JAR 6/26OZ

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

Comercial Mexicana

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…

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

Epitope Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

QUIDEL Sofia SARS Antigen FIA IVD REF 20374

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

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.