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. 2,865 recalls have been distributed to Florida in the last 12 months.
Showing 14301–14320 of 55,837 recalls
Recalled Item: Olanzapine Tablets Recalled by Macleods Pharma Usa Inc Due to cGmp Deviations
The Issue: cGmp Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beckman Coulter IRISpec CA/CB/CC control Recalled by Beckman Coulter, Inc....
The Issue: IRISpec CA failures for glucose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyrazinamide Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Macleods Pharma Usa...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to The photomultiplier...
The Issue: The photomultiplier tube, may have compromised functionality in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProteusPLUS and ProteusONE- designed to produce and deliver a proton...
The Issue: When resuming from a beam pause, the Proton Therapy System does not verify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Software 2.51.01 and Lower - intended Recalled by...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell 8 Square Template Slides (Glass)- microscope slides : PCN008...
The Issue: Labelled with an incorrect expiry date on the outer label with an extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Therapy Air Supply Unit Recalled by Baxter Healthcare Corporation...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE Recalled by...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371 Recalled...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA Drill Bit Recalled by Biomet, Inc. Due to Packaging of various...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Trauma Recalled by Biomet, Inc. Due to Packaging of various implants...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.