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 Aug 12, 2026

munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses…

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

Munevo GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software…

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

Oxos Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…

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

Pride Mobility Products Corp.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number: NCOCO1510 Software Version: N/A…

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

Tissium Sa

7 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 7, 2026Updated Aug 25, 2026

Corte Argentino USA LLC Recalls Raw Beef Products Imported Without The Benefit Of Import Reinspection

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

Corte Argentino USA LLC

USDA FSIS

Medical devices

Reported Aug 5, 2026

L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…

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

Argon Medical Devices, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 5, 2026Updated Sep 16, 2026

Sainforage Sainfoin + Grass + Alfalfa Forage Pellet 40 lb (18.14 KG) UPC: 720260672693. Packaged BOPP woven plastic…

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

Fundamental Feed

2 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Aug 5, 2026

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

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

Permobil Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…

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

ResMed Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.

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

Stryker GmbH

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is a smartphone-based acoustic…

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

Emano Metrics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

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

Kent Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G

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

Medline Industries, LP

17 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying…

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)

Medical devices

Reported Jul 29, 2026

Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT

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

Penumbra, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description:…

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

Prismatik Dentalcraft, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

SeaSpine Polyaxial Head REF Number: 41-3010

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2026

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.…

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 22, 2026

Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen

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

Frutas y Hortalizas del Sur S.A.

FDA (openFDA food enforcement)

Food

Reported Jul 22, 2026

Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4.…

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

General Mills James Ford Bell Technical Center

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2026

da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 22, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

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

LifeSouth Community Blood Centers, Inc.

FDA (weekly enforcement report)

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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.