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 Jan 11, 2023
Liquid Assayed Specific Protein- In vitro diagnostic use, in the quality control of serum on clinical chemistry and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo Soi S- 50x2.5 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tai Phat Wholesalers LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2023
Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2023
"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 4, 2023
Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. (280g) UPC 074410366414 Ingredients: Fish meat (bream,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wismettac Asian Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 4, 2023
XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow Goodness), 12oz. marshmallow fluff, 4 12oz. retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.XO Marshmallow, LLC
FDA (openFDA food enforcement)
Reported Dec 28, 2022
InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Companion Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2022
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allison Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARROW INTERNATIONAL Inc.
32 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml, Total Volume 8 ml in 10 ml syringe, 5-count syringes packaged in a bag…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy
FDA (openFDA drug enforcement)
Reported Dec 21, 2022
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
155 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA drug enforcement)
Reported Dec 14, 2022
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bunnell, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dewei Medical Equipment Co. Ltd.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea
High riskUsing this product could cause serious injury, illness or death — stop using it now.Green Day Produce
FDA (openFDA food enforcement)
Reported Dec 14, 2022
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants 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.