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 May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Accula SARS-CoV-2 Test, REF: COV4100

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

Mesa Biotech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Philips Hemodynamic Application, Model Number 722463, Software Version Number: R1.2.2 and R1.2.3. For visualization and…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model…

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

Proterixbio

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

'KORICA' ROASTED PEANUT; 10.6OZ (300G); packaged in plastic bags; Ingredients: Peanuts, Salt, Licorice, Anise,…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Diagnostic Kit SARS-cCo V Antigen Rapid Test

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

USA Medical, LLC

FDA (openFDA device enforcement)

Food

Reported May 11, 2022

Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract,…

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

A & C Best Food Trading

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 11, 2022

WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515…

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

Bakkavor Foods USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 11, 2022

TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2022

Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test

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

SML Distribution, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

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

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300…

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

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported May 4, 2022

Kinder Happy Moments Kinder Chocolate and Crispy Wafers Assortment 14.1 OZ (400g) square box with lid. Best by: July…

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

Ferrero USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems with either of the following assays:…

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

NeuMoDx Molecular Inc.

FDA (openFDA device enforcement)

Drugs

Reported May 4, 2022

Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc., Preferred Pharmaceuticals, Inc.

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

Preferred Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Food

Reported May 4, 2022

Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 00821 1, Manufactured by Rebel Creamery LLC, Midway, UT 84049.…

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

Rebel Creamery

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

TearCare version 1.0 SmartHubs

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

Sight Sciences, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010

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

Acumed LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.

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

Baxter Healthcare Corporation

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.