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 13, 2018
Bivona¿ Tracheostomy Tube Tracheostomy Tubes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jun 13, 2018
VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VGI Medical, LLC
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Disposable Drill Kit which includes two drill bits, two drill stops, and two adjustment wrenches, sterile. The drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Alfalfa Seeds
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caudill Sprouting LLC
FDA (openFDA food enforcement)
Reported Jun 6, 2018
Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Acmi, Incorporated
FDA (openFDA device enforcement)
Reported Jun 6, 2018
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Datascope Corp. - Cardiac Assist Division
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens, Warrensville Hts., OH 44128 UPC 0-36232-01871-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Hickory Harvest Brand Products Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 6, 2018
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 6, 2018
LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torax Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ziyad Brothers Importing, Inc.
FDA (openFDA food enforcement)
Reported May 30, 2018
iChem VELOCITY Automated Urine Chemistry System, Catalog #700-7176-001 and iChem VELOCITY Automated Urine Chemistry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported May 30, 2018
Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 30, 2018
Hot Dog Buns
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flowers Bakery Of Montgomery LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grand Canyon Foods International LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spinal Elements
FDA (openFDA device enforcement)
Reported May 30, 2018
Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported May 23, 2018
Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott
FDA (openFDA device enforcement)
Reported May 23, 2018
Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aidarex Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported May 23, 2018
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…
High riskUsing this product could cause serious injury, illness or death — stop using it now.eBars
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 23, 2018
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epic Extremity, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
3 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.