Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,768 recalls have been distributed to Florida in the last 12 months.
Showing 18641–18660 of 30,686 recalls
Recalled Item: Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws Recalled by...
The Issue: Incorrect direct marking and color identification for the affected lot of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...
The Issue: Specific lots have been reported to produce falsely lower than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...
The Issue: Teleflex Medical is recalling the affected product because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...
The Issue: The "Retry" command does not function properly which could cause a shortage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Power Drill Torque Limiter Recalled by Orthofix Srl Due to The...
The Issue: The power drill torque limiter may break during use in surgery application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...
The Issue: A small number of batches may crack or break if exposed to certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled...
The Issue: Three (3) complaints were identified in which the potential for utilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID Medical QA Pack AV10654-10 Recalled by Avid Medical, Inc. Due to The...
The Issue: The swab stick collection device provided in a convenience kit expires prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.