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 48,122 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Aug 26, 2020
Smart Stapes Protheses Piston 0.4mm X 5.25 mm- Partial Ossicular Replacement Catalog Number: 70142168
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Calcaneus Plate, Extensile, Small, Left, Catalog Number CPF 101 - Product Usage: intended to be used for internal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Proteus 235 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Aug 19, 2020
AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Linet Americas
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Tibial knee prosthesis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellements LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Mako Hip End Effector, Variable Angle Catalog Number: 206967 GTIN:00848486022167
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Provident Nutraceutical div.
FDA (openFDA food enforcement)
Reported Aug 12, 2020
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sutter Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Salmon cut and packaged in Styrofoam case approximately 19 kg per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Topway Enterprises, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2020
Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Aug 5, 2020
ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 Spine System is intended for immobilization…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Uvt Inc.
FDA (openFDA drug enforcement)
Reported Jul 30, 2020
JBS Food Canada ULC Recalls Raw Boneless Beef Products Distributed without Benefit of Import Re-inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Balter Meat Company
USDA FSIS
Reported Jul 29, 2020
Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
13 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.