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. 2,918 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,918 in last 12 months

Showing 50215040 of 30,686 recalls

Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· Zimmer Surgical Inc

Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...

The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 3.0T Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Intera 1.5T Recalled by Philips North America Due to An incorrect electrical...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Aesculap Inc

Recalled Item: MB362R - JACOBSON DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc...

The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Aesculap Inc

Recalled Item: MB215R - MILLS DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc Due...

The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing