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 Feb 12, 2025
Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Medical Technologies GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
. Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP 4.0x11mm . Nobel Biocare N1 TiUltra TCC RP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare
FDA (openFDA device enforcement)
Reported Feb 12, 2025
Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oxoid Limited
FDA (openFDA device enforcement)
Reported Feb 12, 2025
Greenwise Organic Pecan Halves 8 ounce, plastic printed package marked with lot # 18228 and with a best by date of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pecan Star & Nut Corp.
FDA (openFDA food enforcement)
Reported Feb 12, 2025
IntelliBridge EC10 Module. Model Number: 865115
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
LIFEPAK 35 ECG cable REF 11111-000041
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2025
Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2025
Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BakeMark USA LLC.
FDA (openFDA food enforcement)
Reported Feb 5, 2025
BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Infinity Central Station. Model Number: MS26800 The Infinity CentralStation (ICS) is intended for centralized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iovate Health Sciences USA Inc.
FDA (openFDA food enforcement)
Reported Feb 5, 2025
Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2025
Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2025
NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
KIRKLAND Signature Smoked Salmon NET WT 340 g (12 oz) MUST KEEP REFRIGERATED. INGREDIENTS: Atlantic Salmon (Salmo…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Acme Smoked Fish Corp.
FDA (openFDA food enforcement)
Reported Jan 29, 2025
Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
BD PCR Cartridges used with MAX System. Model Number: 437519
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Mr. Bing brand Sriracha Chili Sauce; 9 oz and 18 oz, in clear PET bottle with green cap; UPC 850044819072 and UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mr Bing Foods Inc.
FDA (openFDA food enforcement)
Reported Jan 29, 2025
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
FDA (openFDA device enforcement)
Reported Jan 22, 2025
McKesson Cardiology Hemo software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.A L I Technologies Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
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.