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. 2,723 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,723 in last 12 months

Showing 2590125920 of 55,837 recalls

DrugNovember 27, 2018· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Aprepitant Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Shortfill: Aprepitant capsules 40 mg is being recalled due to customer...

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

Class III — Low RiskOngoing
Refund
DrugNovember 27, 2018· Teva Pharmaceuticals USA

Recalled Item: Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles Recalled...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 27, 2018· Gemini Food Corporation Inc

Recalled Item: Imperial Taste Fried Garlic Recalled by Gemini Food Corporation Inc Due to...

The Issue: Investigation of consumer complaint found that two products had undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 27, 2018· Gemini Food Corporation Inc

Recalled Item: Imperial Taste Fried Red Onion Recalled by Gemini Food Corporation Inc Due...

The Issue: Investigation of consumer complaint found that two products had undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2018· Smiths Medical ASD Inc.

Recalled Item: ProtectIV¿ Plus Safety IV Catheter Recalled by Smiths Medical ASD Inc. Due...

The Issue: Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 23, 2018· Philips North America LLC

Recalled Item: HeartStart MRx Recalled by Philips North America LLC Due to Affected...

The Issue: Affected lithium-ion batteries may contain a defective component (Thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Progesterone Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i 25-OH Vitamin D Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Free T4 Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Estradiol Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Total Beta-hCG Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i TSH Reagent Kit Recalled by Abbott Ireland Diagnostics Division...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Ferritin Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...

The Issue: Due to a manufacturing variation in the arm that can result in a persistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...

The Issue: Due to a manufacturing variation in the arm that can result in a persistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2018· Abbott

Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...

The Issue: The device is unable to pair with the mobile app due to the device...

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

Class II — Potential Health HazardOngoing