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. 1,819 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,819 in last 12 months

Showing 4556145580 of 55,837 recalls

Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM RESANO FORCEPS Recalled by Intuitive Surgical, Inc. Due to Deviations in...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM PERMANENT CAUTERY SPATULA 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Elekta, Inc.

Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...

The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM PERMANENT CAUTERY HOOK 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 3, 2014· House Of Spices (india) Inc.

Recalled Item: LAXMI NUTKHHAT Golden Raisins Recalled by House Of Spices (india) Inc. Due...

The Issue: The product contained undeclared sulfites based on sampling and analysis by...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 31, 2014· Unity Groves Corporation

Recalled Item: Avocado label: Unity Groves Avocados # 4221 Born in the Recalled by Unity...

The Issue: FDA sample positive for Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 31, 2014· Accuray Incorporated

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2014· Medtronic Perfusion Systems

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2014· US Endoscopy Group Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2014· Alcon Research, Ltd.

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.

Class II — Potential Health HazardOngoing