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 48,196 notices were distributed nationwide, so they reach Florida too — those are in the archive.

Medical devices

Reported Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

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

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 28, 2017

Gourmet Classic Salads, Inc Recalls Ready-To-Eat Meat and Poultry Products Due To Possible Listeria Contamination

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

Gourmet Classic Salads, Inc.

USDA FSIS

Medical devices

Reported Feb 22, 2017

Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder…

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

Allen Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20

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

Bwi Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Feb 22, 2017

Fratelli Beretta USA, Inc. Recalls Mortadella Product Due To Misbranding and Undeclared Allergens

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

Fratelli Beretta USA, Inc.

USDA FSIS

Medical devices

Reported Feb 22, 2017

Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

BrightView XCT

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Pizza Hut Creamy Alfredo sauce, case size 40 lbs. 8 bags per case. Bags are each 80 oz (5 lbs) of sauce

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

Yum Retaurants International

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2017

Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics…

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

Angiodynamics Inc. (Navilyst Medical Inc.)

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 15, 2017

Bon Ton-Sour Cream & Onion Flavored Potato Chips sold in 2.75 oz, 1.5 oz. bags

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

Bickel's Snack Foods Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2017

Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 15, 2017

Century Packing Corp. Recalls Chicken Sausage Products Due To Misbranding

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

Century Packing Corp.

USDA FSIS

Food

Reported Feb 15, 2017

Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17 Net Wt: 10 lb (2-5lb bags)

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

Dutch Valley Food Distributors Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2017

Empowr PS Knee Tibial Insert; Model 343-14-709 The EMPOWR PS tibial insert are made from Highly Cross-Linked Vitamin E…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Bariatric Bed - BAR600IVC

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

Invacare Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

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

Merge Healthcare, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Feb 15, 2017

DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421

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

The Dannon Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2017

InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I non-sterile…

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

Vertebral Technologies, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 15, 2017

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…

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

VistaPharm, Inc.

FDA (openFDA drug 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.