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 2522125240 of 30,686 recalls

Medical DeviceNovember 10, 2014· GE Inspection Technologies, LP

Recalled Item: GE Optional Laser Centering Device X-ray generator. Recalled by GE...

The Issue: GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...

The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· CSA Medical

Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...

The Issue: An increase in complaint trending for a loss of audible sound associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal DX/HX/EX model number: 881001 IntelliSpace Portal...

The Issue: Software defect. In certain circumstances, the application may display...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Breas Medical AB

Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...

The Issue: Unintended treatment termination could result from a keypad malfunction in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...

The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: CONMED ADULT R2 Multifunction Electrodes Recalled by ConMed Corporation Due...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Abbott Medical Optics Inc (AMO)

Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...

The Issue: AMO has received complaints where the finger grip dislodged while depressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...

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

Class II — Potential Health HazardOngoing