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.
Reported Mar 6, 2024
Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ancient Formulas, Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lakeview Farms LLC
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Neurosurgery
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2024
MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mutti USA Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Parker Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Cotija cheese packaged in the following configurations: 1. Sargento Course Grated Cotija Cheese Pack Size 6/5 lb.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sargento Foods, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2024
USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United Orthopedic Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2024
VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) REF PRT-01013-000 with pouch REF PRT-00802-001). Used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ventec Life Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2024
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
FDA (openFDA device enforcement)
Reported Feb 28, 2024
HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMD Medicom Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2024
Baxter Exactamix Pro 1200, REF EXM12DY
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2024
Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 100001002017
High riskUsing this product could cause serious injury, illness or death — stop using it now.Compass Group USA, Inc.
FDA (openFDA food enforcement)
Reported Feb 28, 2024
AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MRP, LLC dba Aquabiliti
FDA (openFDA device enforcement)
Reported Feb 28, 2024
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
FDA (openFDA food enforcement)
Reported Feb 28, 2024
Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Windstone Medical Packaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Gluten Free Bean and Cheese Burrito (5.5 oz), individual plastic overwrap, 12 retail units/case, frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported Feb 21, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2024
HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM 350P/350-UNIT-US-10, 350-STR-US-10,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuroLogica Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Accessory Sets Syringes: 6ml syringe with a female luer with 15cm sealed SCD tubing, REF: RF-T15, and 60ml syringe on a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
CombiDiagnost R90 1.0 (709030)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
1 more product in this recall
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.