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.
Reported Jun 1, 2016
RayStation Therapy Treatment Planning System Stand-alone Software 3.0, 3.5, 4.0, 4.5 and 4.7., designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
FDA (openFDA device enforcement)
Reported Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following labels: 1) Net Wt 6.5 oz, 2) Net Wt 2 lbs, 3) Net…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Sausage Maker, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2016
Taylor Farms Florida Inc. Recalls Salads Containing Chicken Due To Misbranding and Undeclared Allergens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms Florida, Inc.
USDA FSIS
Reported May 25, 2016
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamedix Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Msu Dept Of Fd Sci Dairy Plant
FDA (openFDA food enforcement)
Reported May 25, 2016
Manischewitz Pistachio Orange Macaroons 10 oz. Distributed by: The Manischewitz Company Newark, NJ 07105 Product of USA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.R.A.B. Food Group LLC
FDA (openFDA food enforcement)
Reported May 25, 2016
ADVIA Chemistry Triglyceride_2, concentrated; TRIG_c; Catalog # SMN # 10697575. For in vitro diagnostic use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2016
Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 18, 2016
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
FDA (openFDA device enforcement)
Reported May 18, 2016
Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom Unite Connect for Nurse Call (version 2.2.0).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascom US, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Atlas Spine Torque Limiting Handle 6N-m, P/N 70089 Model # ITN-001-000 Used to rotate implant into position
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atlas Spine, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bradshaw Medical Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 18, 2016
Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) bottle, over the counter, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sesderma, SL
9 more products in this recall
FDA (openFDA drug enforcement)
Reported May 18, 2016
Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q, CD2411-36C, CD1411-36Q, CD1411-36C Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported May 11, 2016
TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L Serial # >200318 and < 2039222 The Dialog+ can be…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B Braun Medical Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
Classic Creme Cookies, Net wt. 12 oz cartons, 6 cartons per case. Manufactured for Back To Nature Foods Co., LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.Back To Nature Foods, LLC
FDA (openFDA food enforcement)
Reported May 11, 2016
Poly-bags containing splint strap labeled with "Pediatric" sticker. Each strap kit contains adjustable length leg…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
GE, Revolution CT. The system is intended for head, whole body, cardiac, and vascular X-ray Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported May 11, 2016
ALFALFA SEED, NET WT. 50 LB. International Specialty Supply LLC, Cookeville, TN
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holding Inc.
FDA (openFDA food 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.