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 Jul 2, 2025
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Limacorporate S.p.A
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Spectral CT. Computed tomography X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jun 25, 2025
CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakkavor Foods USA, Inc.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Medical Corporation
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Yerba Prima Inc.
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode#…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Comvita USA Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipman Family Farms
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microtek Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Mobility LLC
FDA (openFDA device enforcement)
Reported Jun 18, 2025
EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quantum Surgical Sas
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sysco Corporation
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turncare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Access Testosterone assay, Catalog Number 33560
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bedner Growers, Inc.
FDA (openFDA food enforcement)
Reported Jun 11, 2025
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GNC Holdings LLC
FDA (openFDA food 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.