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 Dec 30, 2020

Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

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

Nova Ortho-Med Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2020

Organic fresh cut basil packaged in plastic clamshell containers The Fresh Market Organic Basil NET WT 0.5oz (14g),…

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

Shenandoah Growers, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 30, 2020

Organic Basil,15 bags, Net. Wt.15Lbs case.

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

Vallarta Organics LLC

FDA (openFDA food enforcement)

Drugs

Reported Dec 23, 2020

CJC-1295, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

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

Advanced Nutriceuticals, LLC

16 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 23, 2020

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…

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

Carl Zeiss Meditec AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF…

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

Galt Medical Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 23, 2020

Holiday Cookie Platter packaged in plastic container 20 OZ (1.25 LB) 567g. UPC 41415 88690

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

George DeLallo Co. Inc. New Stanton Warehouse and Production

FDA (openFDA food enforcement)

Medical devices

Reported Dec 23, 2020

Microsurgical Operating Room Tables;7300B (18-350-70);

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

Mizuho America, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular…

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

Ra Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

MAC VU360, Electrocardiograph

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

On the Go Sweet & Salty Trail Mix

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

Kanan Enterprises Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -…

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

Shimadzu Medical Systems

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

PROKERA, non-sterile - Product Usage: Biologic corneal bandage.

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

TissueTech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

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

Welch Allyn, Inc/mortara

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers:…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or…

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

CME America, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01…

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

Janus Trade Group

FDA (openFDA device enforcement)

Drugs

Reported Dec 9, 2020

Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715),…

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

Lohxa LLC

FDA (openFDA drug 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.