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. 2,832 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,832 in last 12 months

Showing 1524115260 of 30,686 recalls

Medical DeviceFebruary 13, 2019· Bioventus, LLC

Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...

The Issue: The firm became aware of the potential for the products' sterile pouch to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e700 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e600 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e500 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...

The Issue: Packaged with an incorrect size inner cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...

The Issue: Incorrect needle length and gage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Fenwal Inc

Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...

The Issue: The optional Vacuum Unit may stop working and display the failure message...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Riverpoint Medical, LLC

Recalled Item: Riverpoint Medical 18G Brachy Grid Recalled by Riverpoint Medical, LLC Due...

The Issue: The integrity of the sterile grid packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Canon Medical System, USA, INC.

Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...

The Issue: Table tilts without operator involvement as a result of liquid spilling into...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Needle Recalled by Terumo Medical Corporation Due to There is a...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Terumo Medical Corporation

Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...

The Issue: There is a potential for a loss of package integrity that may compromise the...

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

Class II — Potential Health HazardOngoing