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 48,132 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Apr 17, 2019
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Commercial Breader Batter; A28177 BATTER MIX X1; 50 pound bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newly Weds Foods Inc.
30 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 17, 2019
Azurion FlexArm, 722079
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2019
AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Procept Biorobotics Corporation
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Losartan 50mg Tablet, 30 count each blister card.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported Apr 17, 2019
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Beaver Visitec
FDA (openFDA device enforcement)
Reported Apr 10, 2019
The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog…
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 Apr 10, 2019
Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Century Snacks LLC
FDA (openFDA food enforcement)
Reported Apr 10, 2019
McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cypress Medical Products LLC
FDA (openFDA device enforcement)
Reported Apr 10, 2019
e500 Automatic Transport Ventilator, Model Number 01EVE500
High riskUsing this product could cause serious injury, illness or death — stop using it now.O-Two Medical Technologies, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
Premium Sustainable Atlantic Salmon (Farm Raised); 22 lb. case - Master carton - corrugated cardboard box. Internal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Procesadora Aguas Claras LTDA.
FDA (openFDA food enforcement)
Reported Apr 3, 2019
Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avitus Orthopaedics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Modjeskas Bauer's Candies NET WT 8 oz, 12 oz, 16 oz, 32 oz. boxes & 4 oz, 8 oz bags, 400 pc case, 216 pc case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bauer's Candies, Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 3, 2019
BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jacques Torres Manufacturing , llc.
FDA (openFDA food enforcement)
Reported Apr 3, 2019
Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Fullei Fresh brand Organic Mung Bean Sprouts in a 4 oz. clear plastic clamshell container
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kwokcheng Enterprise, Inc. dba Fullei Fresh
FDA (openFDA food enforcement)
Reported Apr 3, 2019
Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2019
Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horizon Food Group
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 27, 2019
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90 count bottles, Rx Only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Macleods Pharma USA Inc.
FDA (openFDA drug 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.