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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 2640126420 of 55,837 recalls

Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 4mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda Freestanding Warmer. Device sold under the following product names:...

The Issue: Potential electric leakage affecting the user.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
FoodSeptember 25, 2018· Whole Foods Market

Recalled Item: 365 Everyday Value Brand White Corn Chips Recalled by Whole Foods Market Due...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 24, 2018· Harris Teeter

Recalled Item: Harris Teeter Low Fat FROZEN YOGURT cookies & cream 1.5 Recalled by Harris...

The Issue: The firm was notified by a customer of peanut butter cups in the product....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...

The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing