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. 2,911 recalls have been distributed to Florida in the last 12 months.
Showing 5721–5740 of 30,686 recalls
Recalled Item: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System Recalled by...
The Issue: Device packaged inside an incorrect outer box; displaying artwork &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit-For in vitro diagnostic use Recalled by...
The Issue: During an internal audit a small percentage (<10%) of plastic caps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists...
The Issue: Eye syncing issues causing the device to be inoperable. Unable to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Dry Seal Chest Drains (Express): 4000-100N DRAIN Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Prime Plus Analyzer -Intended to measure certain gases in...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drains (Ocean): Products Product Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235. PTS-11 versions Recalled by Ion...
The Issue: The patient positioning system can perform motions in unexpected directions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure Recalled...
The Issue: Potential risk of reporting erroneous creatinine patient results associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senhance Surgical System Recalled by Asensus Surgical Inc Due to Asensus...
The Issue: Asensus Surgical has identified a malfunction that has occurred and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCU Recalled by CareFusion 303, Inc. Due to Alaris PCA Module...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module 8120 Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptima CMV Quant Assay Recalled by Hologic, Inc. Due to Use of assay along...
The Issue: Use of assay along with plasma specimen may result in error code which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Video System Center Model Number CV-190. Intended Recalled by...
The Issue: Certain serial numbers of the CV-190 do not start up properly because parts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.