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. 2,801 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,801 in last 12 months

Showing 1748117500 of 30,686 recalls

Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· Ethicon, Inc.

Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...

The Issue: Products labeled for distribution outside the United States may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Synthes, Inc.

Recalled Item: Flex Arm Product Usage: The Synthes Flex Arm is a Recalled by Synthes, Inc....

The Issue: Quick connect feature of instruments may be unable to connect to the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Estradiol Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Control Recalled by Tosoh Bioscience Inc Due to The...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Recalled by Tosoh Bioscience Inc Due to The assay...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Calibrator Recalled by Tosoh Bioscience Inc Due to...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Pretreatment Solution Recalled by Tosoh Bioscience...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Testosterone Recalled by Tosoh Bioscience Inc Due to Asfotase...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Cort Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Prolactin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK FSH Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK CA 19-9 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing