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 Nov 18, 2020

Niobe ES System, Models 001-006000-1 and 001-006100-1

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

Stereotaxis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, for the following…

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

XTANT Medical

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2020

Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter…

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2020

Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Drugs

Reported Nov 11, 2020

Metformin HCL E/R 500 mg, 90 Tabs, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 NDC 72189-064-90

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

Direct Rx

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 11, 2020

Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2020

A Li-Gator Single Use Laparoscopic Clip Applier, 10 mm X 29 cm - Product Usage: intended for use on tubular structures…

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

Genicon, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Nov 11, 2020

metformin HCL ER 500 mg, a) 30 tablets NDC: 72789-009-30; b) 60 tablets NDC: 72789-009-60; c) 90 tablets NDC:…

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

PD-Rx Pharmaceuticals, Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 11, 2020

Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation

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

Primus Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 4, 2020

Equinoxe Platform Fracture Stem, 6.5mm, Left - Product Usage: The Equinoxe Platform Fracture Stem is indicated for…

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 4, 2020

Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head,…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2020

Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…

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

Hadson (Toko) Trading Co., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 4, 2020

Merge LIS

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2020

Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…

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

Nurture Inc. dba Happy Family

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 4, 2020

Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600 - Product Usage: he…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2020

Frozen raw Lobster Tail pastry 100 count, sold in 15LB, 24LB, 40.25LB cases

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

Ariola Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2020

System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…

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

ICU Medical, Inc.

98 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…

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

Smith & Nephew, Inc.

40 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products 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.