All recall categories

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 48,100 notices were distributed nationwide, so they reach Florida too — those are in the archive.

Medical devices

Reported Sep 10, 2025

Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Preat Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

RayStation with the following product descriptions: 1. RayStation 7, Software Version: 7.0.0.19. 2. RayStation 8A,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raysearch Laboratories Ab

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Panko Style Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging, corrugated master cartons. Master carton…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tampa Maid Foods, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 10, 2025

Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SALAD KIT, NET WT. 8.3 OZ (235g), INGREDIENTS: HONEY BALSAMIC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Farms Retail, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Spectrum IQ Infusion Pump, Product Code 3570009

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging, master cartons. Master carton case is 20…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beaver Street Fisheries, Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 3, 2025

Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Blue Bell Creameries, LP

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Deep Sprouted Mat 16 oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Chetak New York LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diagnostica Stago, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS. Canal filling stem implants.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Onkos Surgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

Orascoptic Superior Visualization Custom loupes with Dragonfly frames

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Orascoptic Surgical Acuity

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The J.M. Smucker Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

THOR Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 27, 2025

7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Buffalo Rock Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 27, 2025

Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dynex Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Pentax Medical Video Processor; Model Number: EPK-i8020c;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pentax

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

a.) Actylis brand Lithium Orotate 4% packaged in HDPE Liner in a 25kg carton b.) Actylis brand Lithium Orotate 9%…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Aceto US, L.L.C

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.