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 Oct 26, 2022

Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…

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

Abbott Vascular

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 26, 2022

ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF…

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

ARROW INTERNATIONAL Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 26, 2022

Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.

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

Balt USA, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 26, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…

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

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…

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

Lyons Magnus LLC

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Meat & poultry

Reported Oct 26, 2022

New Universal Nourishment LLC Recalls Beef Burger Patty Products Produced Without Benefit of Inspection

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

New Universal Nourishment LLC

USDA FSIS

Food

Reported Oct 26, 2022

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…

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

Seeking Health LLC

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case…

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

Treehouse Foods

FDA (openFDA food enforcement)

Medical devices

Reported Oct 19, 2022

Veritas Advanced Infusion Packs. Used in ophthalmic procedures.

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 Oct 12, 2022

Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or…

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

Sprigs - Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case

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

Eden's Answers Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

"Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases .

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

Kenover Marketing Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

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

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 12, 2022

Sanitizing Hand Spray 80% (alcohol 80% v/v) Packaged in 2 FL OZ (60 mL) bottles, Salon Technologies International 8810…

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

Salon Technologies International Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Food

Reported Oct 12, 2022

WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods…

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

Vanlaw Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog No.: EVLT55OPS (each box contains 5 Procedure Kits). For…

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A

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

Barco Nv

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark I Benchtop Incubator (AY102295). The Mark…

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

CooperSurgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.

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

DICOM Grid, Inc. d/b/a Ambra Health

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.