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. 2,944 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,944 in last 12 months

Showing 381400 of 55,837 recalls

Medical DeviceDecember 24, 2025· GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

Recalled Item: GE Healthcare Omni Legend Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL...

The Issue: There is a potential intermittent issue on certain Omni Legend systems that...

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

Class II — Potential Health HazardOngoing
FoodDecember 23, 2025· B.C. Williams Bakery Service, Inc

Recalled Item: Swiss Chocolate Cake Mix Recalled by B.C. Williams Bakery Service, Inc Due...

The Issue: Undeclared Milk Allergen

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 23, 2025· B.C. Williams Bakery Service, Inc

Recalled Item: Spice Cake Mix Recalled by B.C. Williams Bakery Service, Inc Due to...

The Issue: Undeclared Milk Allergen

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 23, 2025· B.C. Williams Bakery Service, Inc

Recalled Item: Bread and Roll Mix Recalled by B.C. Williams Bakery Service, Inc Due to...

The Issue: Undeclared Milk Allergen

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 23, 2025· Focalyx Technologies, LLC.

Recalled Item: Focalyx Fusion Recalled by Focalyx Technologies, LLC. Due to Software device...

The Issue: Software device that is an accessory for image-guided interventional and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2025· Beckman Coulter, Inc.

Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...

The Issue: Sample preparation system designed to automate staining, lysing, cell...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2025· Baxter Healthcare Corporation

Recalled Item: Sterile Water for Irrigation Recalled by Baxter Healthcare Corporation Due...

The Issue: Presence of particulate matter: plastic particles from the bottle rim were...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2025· Cipla USA, Inc.

Recalled Item: Diclofenac Sodium Topical Gel Recalled by Cipla USA, Inc. Due to Failed PH...

The Issue: Failed PH Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· LSL Healthcare Inc.

Recalled Item: LSL Healthcare Recalled by LSL Healthcare Inc. Due to BD ChloraPrep Triple...

The Issue: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Philips North America

Recalled Item: Patient Information Center iX Recalled by Philips North America Due to A...

The Issue: A recent software (SW) patch modifies Mobile Event Notification filter...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: traZODONE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA) Inc...

The Issue: Failed Tablet/Capsule Specifications: Product complaint received that some...

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

Class III — Low RiskOngoing
Refund
DrugDecember 19, 2025· Novo Nordisk Inc.

Recalled Item: Wegovy (semaglutide) Injection Recalled by Novo Nordisk Inc. Due to Presence...

The Issue: Presence of Particulate Matter: Hair was found in a prefilled syringe

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2025· Novo Nordisk Inc.

Recalled Item: Wegovy (semaglutide) Injection Recalled by Novo Nordisk Inc. Due to Presence...

The Issue: Presence of Particulate Matter: Hair was found in a prefilled syringe

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

Class II — Potential Health HazardOngoing
Refund