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 Jul 11, 2018
Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E Product CVCs are intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Jul 11, 2018
WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods Service, Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Jul 11, 2018
da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Medical Corp.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Absonutrix
FDA (openFDA food enforcement)
Reported Jul 4, 2018
HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cenorin, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Star Wholesale Inc.
FDA (openFDA food enforcement)
Reported Jul 4, 2018
The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) Proteus 235, Beam Management System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
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)
Reported Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Safe N Simple No-Sting Skin Barrier Film, Ostomy Skin Barrier Wipe, SNS00807
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safe N Simple, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2018
CritiCore Automated Urine Output and Temperature Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
VNS Therapy Programmer, Model 3000, v1.0 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
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.