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 Oct 26, 2016
Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Del Monte Research Center - Walnut Creek
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
FDA (openFDA food enforcement)
Reported Oct 26, 2016
HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
COZY SHRIMP, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kabobs Inc.
26 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for external defibrillation,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Leonhard Lang Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When…
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 Oct 26, 2016
Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: Heavy duty Sagittal Blades are used to cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
PREMIUM PROTEIN III For kids Nutritional Supplement, NET WT 16 OZ (454g), Manufactured for Celwa Biotech Brooklyn, NY…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Triceutical Inc./Zhang
20 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Abdominoplasty Pack, Kit number AMS3326 convenience custom kits used for general surgery in hospital operating room
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
149 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Uniflex Humeral Nail: 467265 G-PIN 2.8BL 3.2PL 60CM 2PK Pin, Fixation, Smooth A 467265-01 Ball Tip Guide Pin is used to…
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 Oct 19, 2016
TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocompatibles U.K., Ltd.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Better-Bladder With 14" ID tubing, ITEM BB14, STERILE, Measure pressure noninvasively in the extracorporeal circuit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Monaco RTP System The Monaco system is used to make treatment plans for patients with prescriptions for external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
OEC Brivo 715 Prime, OEC Brivo 785 Essential, OEC Brivo 865 Advance Product Usage: The OEC Brivo Mobile C-Arm X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Medix NatalCare LX Intensive Care Incubator. Neonatal incubator. Item numbers: DMNCLX1; KITNC-STLX0003;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Radiation Therapy Treatment Planning System, Model 5.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Oct 19, 2016
BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Specialties Mexico S DE RL DE CV
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product 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.