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.

55,837 total recalls
2,710 in last 12 months

Showing 2810128120 of 30,686 recalls

Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201333 Femur CR POR FEM SURF HDN HATCP CML Recalled by Zimmer, Inc. Due...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595201201 Femur CR-FLEX POR FEM B-L Rx Recalled by Zimmer, Inc. Due to...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597202009 Articular Surface CR ART SURF 12/PURPLE 09 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595001201 Femur CR-FLEX PCT FEM B-L Rx Recalled by Zimmer, Inc. Due to...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201303 Femur CR POR FM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due to...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...

The Issue: Medtronic recently identified an issue with a subset of Consulta¿ CRT-P and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing