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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 25281–25300 of 30,686 recalls
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM FENESTRATED BIPOLAR FORCEPS Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...
The Issue: Software upgrade to correct potential safety issue related to CyberKnife...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroSeal Adjustable Endoscopic Valve. Model/Catalog # 00913410 The primary...
The Issue: Packaging non-conformance related to the integrity of the sterile pouch seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Affinity Fusion Oxygenator with Integrated Arterial Filter and Carmeda...
The Issue: Medtronic initiated an Urgent Medical Device Recall for 66 distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM...
The Issue: The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...
The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...
The Issue: It was determined that if the Mammomat Inspiration system is not secured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...
The Issue: Portions of the lots may contain units with an incorrect lens axis condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...
The Issue: Drill set may contain incorrect drill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Troponin I For in vitro diagnostic use for the Recalled by Siemens...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...
The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.