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 48,122 notices were distributed nationwide, so they reach Florida too — those are in the archive.

Medical devices

Reported Nov 15, 2023

DJO EMPOWR Knee Punch Handle, REF: 801-05-040

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

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260

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

Family Dollar Stores, Llc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Gills Onions 3 lb. bags, diced yellow onions

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

Gills Onions, LLC

72 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Nov 15, 2023

V-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioActive Nutritional, Inc., 1803 N. Wickham…

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

Grato Holdings, Inc.

FDA (openFDA drug enforcement)

Food

Reported Nov 15, 2023

Frozen and fresh RTE Lobster meat (1 lb. packages to 12 lb. case) 1. Greenhead Lobster HPP Fresh Cooked Claw and…

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

Greenhead Lobster Products LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

VITROS Chemistry Products Lipase Slides, Product Codes 1668409 (contains 60 Slides per Cartridge) and 8297749 (contains…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model #…

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

Philips Ultrasound, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP

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

Pulmonx, Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

Senhance Surgical System, which includes: Manipulator Arm, ISU Configuration ( Catalog Number X9007708), Intelligent…

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

Asensus Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033,…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU,…

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

Maquet Cardiovascular, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Food

Reported Nov 8, 2023

Nature's Path Organic Pumpkin Spice Waffles, 7 oz., UPC 0 5844959077 4

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

Nature'S Path Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 8, 2023

Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…

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

Quest Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

General Pack, REF BBGP31C

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

American Contract Systems, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…

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

Betty Lou's Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

SOZO Bilateral Arm L-Dex Software

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

Impedimed Limited

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor

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

Orgain

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental

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

Preat Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

Astral 100 and Astral 150 ventilators

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

ResMed Ltd.

FDA (openFDA device enforcement)

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Other states

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.