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. 2,904 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,904 in last 12 months

Showing 70217040 of 55,837 recalls

Medical DeviceFebruary 19, 2024· ConvaTec, Inc

Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...

The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2024· Global Corporation

Recalled Item: Broncochem Cold & Flu Syrup Kids (acetaminophen Recalled by Global...

The Issue: Stability testing failures for one or two of the four active pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2024· Global Corporation

Recalled Item: Broncochem Cold & Tea (acetaminophen Recalled by Global Corporation Due to...

The Issue: Stability testing failures for one or two of the four active pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Ten 10ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Medivance Inc.

Recalled Item: Medivance Neonatal ArcticGel Pads Recalled by Medivance Inc. Due to Neonatal...

The Issue: Neonatal pads are experiencing reduced water flow, which may reduce or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Medtronic Inc.

Recalled Item: Abre Venous Self-expanding Stent System Recalled by Medtronic Inc. Due to...

The Issue: There is a potential for sterile package breach.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Biosense Webster, Inc.

Recalled Item: CARTO VIZIGO Bi-Directional Guiding Sheath Recalled by Biosense Webster,...

The Issue: Due to a manufacturing issue, device under process validation phase were...

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

Class II — Potential Health HazardOngoing
FoodFebruary 15, 2024· Turkana Food Inc.

Recalled Item: Sekeroglu Lokum Love Turkish Delight Mixed With Pistachio And Pomegranate...

The Issue: Product contains Acid Red 18

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2024· Turkana Food Inc.

Recalled Item: Sekeroglu Lokum Love Turkish Delight With Pistachio And Pomegranate Flavor...

The Issue: Product contains Acid Red 18

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2024· Eugia US LLC

Recalled Item: Methocarbamol Injection Recalled by Eugia US LLC Due to Presence of...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2024· Philips North America Llc

Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...

The Issue: If the DIVA touch display generates touch inputs without user interaction,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Mariner RDX Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION Due...

The Issue: Screw heads, of pedicle screw systems, have thin lead-in thread that pose a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing