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 3034130360 of 55,837 recalls

FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Ginger Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Pineapple Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cherries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Ginger Snap Cookies Recalled by GKI Foods, LLC Due to...

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Banana Chips Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Coconut Almonds Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cashews Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cranberry Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Peanuts Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Powerberry Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Strawberries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 26, 2017· ConvaTec, Inc

Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...

The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2017· Zimmer Biomet, Inc.

Recalled Item: fastener Recalled by Zimmer Biomet, Inc. Due to It was identified that the...

The Issue: It was identified that the product was not assembled correctly causing the...

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

Class II — Potential Health HazardOngoing