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. 2,178 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,178 in last 12 months

Showing 50415060 of 30,686 recalls

Medical DeviceDecember 28, 2023· NeuroLogica Corporation

Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...

The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...

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

Class II — Potential Health HazardOngoing
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· MRP, LLC dba Aquabiliti

Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...

The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· Maquet Medical Systems USA

Recalled Item: Bubble Sensor (.5720) Recalled by Maquet Medical Systems USA Due to The...

The Issue: The Bubble Sensor optional accessory to the CARDIOHELP-i extracorporeal life...

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

Class II — Potential 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...

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...

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 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: IFU has been updated to include warnings about the risk of the inlet...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: New warnings are being added to the Instructions for Use for all affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2023· TruAbutment Inc.

Recalled Item: Brand Name: TruScan Body Recalled by TruAbutment Inc. Due to Retroactive:...

The Issue: Retroactive: Due to defect and quality issues dental scanner may not scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· GE Medical Systems, SCS

Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...

The Issue: X-ray exposure termination audible signal on Senographe Pristina with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Solutions Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: Sterility assurance for saline included in surgical kits cannot be guaranteed.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Solutions Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: Sterility assurance for saline included in surgical kits cannot be guaranteed.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Solutions Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: Sterility assurance for saline included in surgical kits cannot be guaranteed.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Solutions Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: Sterility assurance for saline included in surgical kits cannot be guaranteed.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 1200 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 2400 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing