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 Nov 23, 2016
MEVION S250 Product Usage: Proton Radiation Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Model 208-70-110, Long Thread Tiger Large Cannulated Headless Screw, 7 x 110 mm labeled as "7.0 x 110mm LTTHCS REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Nov 18, 2016
Wayne Farms, LLC Retira Productos De Pechuga De Pollo Listos Para Comer Los Cuales Podran Estar Medios Crudos
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Nov 16, 2016
Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.1 Epic, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 16, 2016
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Iberia Codfish Fritter Mix
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Productos La Finca, Inc.
FDA (openFDA food enforcement)
Reported Nov 16, 2016
ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reshape Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schaerer Medical USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International, Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Rigid Suction Canister 3000 CC and 2000 CC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Visualase Visualization Stylets PN 020-2301. The individual components within the Visualase Body Accessory Kit are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Select Recipe Buttermilk Ranch Dressing, Net contents: 1 GAL (3.79 L), 4 X 1 GAL
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Oasis Foods Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2016
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
The PAXWIRE Occlusion Balloon System consists of an occlusion catheter, inflation handle and syringes. It is designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AccessClosure, Inc., A Cardinal Health Company
FDA (openFDA device enforcement)
Reported Nov 2, 2016
BRACH'S Chocolate Creations, Milk Chocolate Almond Supremes, Fresh roasted almonds drenched in rich creamy milk…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ferrara Candy Comp
FDA (openFDA food enforcement)
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
22 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 2, 2016
VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sequent Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TZ Medical, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Cetylev (acetylcysteine) effervescent tablets for oral solution, 500 mg, Rx Only, 20 tablets per carton (ten 2 count…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arbor Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
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.