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. 2,754 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,754 in last 12 months

Showing 2036120380 of 30,686 recalls

Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...

The Issue: Accuray has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2016· Acumed LLC

Recalled Item: OPT Croutons is a synthetic bone substitute designed for the Recalled by...

The Issue: OPT Croutons, part number 65-0210-S, is recalled due to the result of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...

The Issue: Edits to Particle field definition parameters may not be saved when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Mckesson Medical Imaging

Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...

The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...

The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Varian Medical Systems, Inc.

Recalled Item: Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart...

The Issue: Modifications in version 13.6MR2 for Contouring, SmartAdapt, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...

The Issue: Reunion TSA Peg Alignment Sound broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing