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. 2,654 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,654 in last 12 months

Showing 4200142020 of 55,837 recalls

Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Optical Access System Recalled by Stryker Sustainability Solutions Due to...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Elekta, Inc.

Recalled Item: Laksell GammaPlan Recalled by Elekta, Inc. Due to Memory can become...

The Issue: Memory can become corrupted when creating a fused study via drag and drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2015· Merge Healthcare, Inc.

Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...

The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...

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

Class II — Potential Health HazardOngoing
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMay 29, 2015· Kerry Foods

Recalled Item: Kraft Non-Dairy Creamer Recalled by Kerry Foods Due to Kerry, Inc. is...

The Issue: Kerry, Inc. is voluntarily recalling all Nondairy Creamer produced between...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 29, 2015· Kerry Foods

Recalled Item: Kraft French Vanilla Recalled by Kerry Foods Due to Kerry, Inc. is...

The Issue: Kerry, Inc. is voluntarily recalling all Nondairy Creamer produced between...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 29, 2015· Walgreen Company

Recalled Item: Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a Recalled by Walgreen...

The Issue: Nice! Powdered Sugar Mini Donuts may contain mold. Alleged illnesses have...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 29, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System software RayStation is a...

The Issue: An error caused by a floating point precision problem tends to cause a...

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

Class II — Potential Health HazardOngoing