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 48,132 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Jun 27, 2018
Nitinol Staple, Elastic Staple Large-Asymmetrical, Sterile R, Model #: a) ES-18x15x17; b) ES-18x17x19
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2018
Agri Star Meat And Poultry Llc Retira Productos De Pastrami De Carne De Res Debido A Una Posible Desviacin Durante El…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agri Star Meat and Poultry, LLC
USDA FSIS
Reported Jun 20, 2018
lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego Inc. dba Immunalysis Corporation
FDA (openFDA device enforcement)
Reported Jun 20, 2018
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
37 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the following products: CellaVision DM96, DM1200, DM9600…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cellavision AB
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035 Product Usage: The Maquet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morley Candy Makers, Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Century Snacks LLC
FDA (openFDA food enforcement)
Reported Jun 20, 2018
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.R.A.B. Food Group LLC
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Part #: SAM XT-M, Model: Tactical Black or Military
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Seaberg Company Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Priano Rosso Pesto Sauce, 6.7oz glass jar
High riskUsing this product could cause serious injury, illness or death — stop using it now.BLM Products U. Vertriebsges
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Desly International Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH PITT, NET WT. 1 LB, and 0.50 LB, PRODUCE OF PAKISTAN,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Global Commodities Inc.
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lake Michigan Distilling Co. LLC
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Restoris MCK Onlay Insert Extractor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix, Inc.
19 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.